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Items: 1 to 20 of 28

1.

Homo sapiens isolate CHM13 chromosome 7, alternate assembly T2T-CHM13v2.0

160,567,428 bp linear DNA

Accession:
NC_060931.1
GI:
2194973865
2.

Homo sapiens isolate CHM13 chromosome 7

160,567,428 bp linear DNA

Accession:
CP068271.2
GI:
2033700209
3.

Homo sapiens homeobox A3 (HOXA3), transcript variant 14, mRNA

2,575 bp linear mRNA

Accession:
NM_001384346.1
GI:
1858900757
4.

Homo sapiens homeobox A3 (HOXA3), transcript variant 9, mRNA

2,696 bp linear mRNA

Accession:
NM_001384341.1
GI:
1858589288
5.

Homo sapiens homeobox A3 (HOXA3), transcript variant 11, mRNA

2,507 bp linear mRNA

Accession:
NM_001384344.1
GI:
1858589285
6.

Homo sapiens homeobox A3 (HOXA3), transcript variant 5, mRNA

3,071 bp linear mRNA

Accession:
NM_001384337.1
GI:
1858589267
7.
8.

Homo sapiens homeobox A3 (HOXA3), transcript variant 8, mRNA

2,783 bp linear mRNA

Accession:
NM_001384340.1
GI:
1858589259
9.

Homo sapiens homeobox A3 (HOXA3), transcript variant 6, mRNA

2,598 bp linear mRNA

Accession:
NM_001384338.1
GI:
1858589255
10.

Homo sapiens homeobox A3 (HOXA3), transcript variant 7, mRNA

2,899 bp linear mRNA

Accession:
NM_001384339.1
GI:
1858589236
11.

Homo sapiens homeobox A3 (HOXA3), transcript variant 10, mRNA

2,599 bp linear mRNA

Accession:
NM_001384342.1
GI:
1858589227
12.

Homo sapiens homeobox A3 (HOXA3), transcript variant 13, mRNA

2,568 bp linear mRNA

Accession:
NM_001384345.1
GI:
1858589218
13.

Homo sapiens homeobox A3 (HOXA3), transcript variant 4, mRNA

3,188 bp linear mRNA

Accession:
NM_001384336.1
GI:
1858589216
14.

Homo sapiens homeobox A3 (HOXA3), transcript variant 12, mRNA

2,581 bp linear mRNA

Accession:
NM_001384343.1
GI:
1858589214
15.
16.

Homo sapiens homeobox A3 (HOXA3), transcript variant 3, mRNA

3,142 bp linear mRNA

Accession:
NM_001384335.1
GI:
1858589184
17.
18.

Homo sapiens clone Affy08242H09, mRNA sequence

369 bp linear mRNA

Accession:
DQ655986.2
GI:
155574038
19.

Homo sapiens homeobox A3 (HOXA3), transcript variant 3, mRNA

2,773 bp linear mRNA

  • Record suppressed.NM_153632.2: This RefSeq was permanently suppressed because it represents a poorly supported variant with non-consensus splice sites.
Accession:
NM_153632.2
GI:
84043948
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