ID: 55342 | spermatid perinuclear RNA binding protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (123109494..123268586, complement) | HEL162, ILF3L, SPNR, p74 | 611138 |
ID: 29894 | cleavage and polyadenylation specific factor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144393231..144409335, complement) | CPSF160, HSU37012, MYP27, P/cl.18 | 606027 |
ID: 2873 | G protein pathway suppressor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82050932..82057470) | COPS1, CSN1, SGN1 | 601934 |
ID: 23287 | ATP/GTP binding carboxypeptidase 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (85546539..85805483, complement) | CCP1, CONDCA, NNA1 | 606830 |
ID: 1820 | AT-rich interaction domain 3A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (925732..975939) | BRIGHT, DRIL1, DRIL3, E2FBP1 | 603265 |
ID: 27244 | sestrin 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (108984309..109094846, complement) | PA26, SEST1 | 606103 |
ID: 57460 | protein phosphatase, Mg2+/Mn2+ dependent 1H [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (62643994..62935150, complement) | ARHCL1, NERPP-2C, URCC2 | 616016 |
ID: 55829 | selenoprotein S [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (101270809..101277485, complement) | AD-015, ADO15, SBBI8, SELS, SEPS1, VIMP | 607918 |
ID: 166968 | MIER family member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (56919603..56952209, complement) | | 620100 |
ID: 203062 | t-SNARE domain containing 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142212080..142407029, complement) | | |
ID: 317781 | DEAD-box helicase 51 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (132136594..132144319, complement) | | |
ID: 9401 | RecQ like helicase 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144511288..144517833, complement) | RECQ4 | 603780 |