| ID: 622 | 3-hydroxybutyrate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197509783..197573343, complement) | BDH, SDR9C1 | 603063 |
| ID: 3263 | hemopexin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6431049..6440987, complement) | HX | 142290 |
| ID: 735 | complement C9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (39284140..39364495, complement) | ARMD15D, C9 | 120940 |
| ID: 1558 | cytochrome P450 family 2 subfamily C member 8 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (95036772..95069497, complement) | CPC8DM, CYPIIC8, MP-12/MP-20, CYP2C8 | 601129 |
| ID: 763 | carbonic anhydrase 5A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87881549..87936529, complement) | CA5D, CAV, CAVA, GS1-21A4.1, CA5A | 114761 |
| ID: 570 | bile acid-CoA:amino acid N-acyltransferase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101360417..101385006, complement) | BACAT, BACD1, BAT, HCHO | 602938 |
| ID: 2147 | coagulation factor II, thrombin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46719213..46739506) | PT, RPRGL2, THPH1 | 176930 |
| ID: 6554 | solute carrier family 10 member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69775416..69797241, complement) | FHCA2, NTCP | 182396 |
| ID: 256394 | serpin family A member 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94442464..94452800, complement) | | 619619 |
| ID: 140290 | t-complex 10 like [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (32573721..32585523, complement) | C21orf77, LINC00846, PRED77, TCP10A-1, TCP10A-2 | 608365 |
| ID: 1361 | carboxypeptidase B2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (46053186..46105033, complement) | CPU, PCPB, TAFI | 603101 |
| ID: 6360 | C-C motif chemokine ligand 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (35976499..35981497, complement) | CKb12, HCC-4, ILINCK, LCC-1, LEC, LMC, Mtn-1, NCC-4, NCC4, SCYA16, SCYL4 | 601394 |
| ID: 2267 | fibrinogen like 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (17864389..17895538, complement) | HFREP1, HP-041, HPS, LFIRE-1, LFIRE1 | 605776 |
| ID: 3698 | inter-alpha-trypsin inhibitor heavy chain 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (7703316..7749520) | H2P, ITI-HC2, SHAP | 146640 |
| ID: 10599 | solute carrier organic anion transporter family member 1B1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21131194..21239796) | HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 | 604843 |
| ID: 433 | asialoglycoprotein receptor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7101322..7115146, complement) | ASGP-R2, ASGPR2, CLEC4H2, HBXBP, HL-2 | 108361 |
| ID: 6898 | tyrosine aminotransferase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71565660..71577092, complement) | | 613018 |
| ID: 336 | apolipoprotein A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161222292..161223628, complement) | Apo-AII, ApoA-II, apoAII | 107670 |
| ID: 462 | serpin family C member 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (173903800..173917327, complement) | AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2, THPH7 | 107300 |
| ID: 85320 | ATP binding cassette subfamily C member 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (48164819..48247539, complement) | EWWD, MRP8, WW | 607040 |