| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080414.3 | 3144 | Missense Mutation | GCG,GGG | A1976G | NP_001073883.2 |
| XM_005267691.4 | 3144 | Intron | XP_005267748.1 | ||
| XM_011536796.2 | 3144 | Missense Mutation | GCG,GGG | A1940G | XP_011535098.1 |
| XM_017021335.1 | 3144 | Intron | XP_016876824.1 | ||
| XM_017021336.1 | 3144 | Missense Mutation | GCG,GGG | A1003G | XP_016876825.1 |
| XM_017021337.1 | 3144 | Intron | XP_016876826.1 |