| Accession: | NM_001286125 |
|---|---|
| 基因名称: | SLC17A2 |
| 基因别名: | NPT3 |
| 基因描述: | Homo sapiens solute carrier family 17, member 2 (SLC17A2), transcript variant 3, mRNA. |
| 种属: | Human |
| CDS区长度: | 1197 (查看编码区序列) |
| 翻译后氨基酸长度: | 398 (查看氨基酸序列) |
| Transcript Variant: | This variant (3) lacks an alternate exon and uses an alternate splice site, both of which contribute to a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (c) has a distinct C-terminus and is shorter than isoform a. |
| 人 SLC17A2 (NM_001286123) cDNA克隆 | transcript variant 1 |
| 人 SLC17A2 (NM_005835) cDNA克隆 | transcript variant 2 |
| 人 SLC17A2 (NM_001286125) cDNA克隆 | transcript variant 3 |