| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242472.1 | 1350 | Intron | NP_001229401.1 | ||
| NM_001242474.1 | 1350 | Intron | NP_001229403.1 | ||
| NM_001242475.1 | 1350 | Intron | NP_001229404.1 | ||
| NM_001242476.1 | 1350 | Intron | NP_001229405.1 | ||
| NM_003419.4 | 1350 | Intron | NP_003410.1 | ||
| XM_011526704.2 | 1350 | Intron | XP_011525006.1 | ||
| XM_017026568.1 | 1350 | Intron | XP_016882057.1 | ||
| XM_017026569.1 | 1350 | Intron | XP_016882058.1 | ||
| XM_017026570.1 | 1350 | Intron | XP_016882059.1 | ||
| XM_017026571.1 | 1350 | Intron | XP_016882060.1 | ||
| XM_017026572.1 | 1350 | Intron | XP_016882061.1 | ||
| XM_017026573.1 | 1350 | Intron | XP_016882062.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001037232.3 | 1350 | Missense Mutation | GGT,TGT | G329C | NP_001032309.2 |
| NM_001171979.1 | 1350 | Missense Mutation | GGT,TGT | G410C | NP_001165450.1 |
| XM_005258876.4 | 1350 | Missense Mutation | GGT,TGT | G329C | XP_005258933.1 |
| XM_011526933.2 | 1350 | Missense Mutation | GGT,TGT | G329C | XP_011525235.1 |