| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039617.1 | 1015 | Missense Mutation | GCG,GTG | A308V | NP_001034706.1 |
| XM_005269279.2 | 1015 | Intron | XP_005269336.1 | ||
| XM_006713493.2 | 1015 | Missense Mutation | GCG,GTG | A306V | XP_006713556.1 |
| XM_006713494.2 | 1015 | Missense Mutation | GCG,GTG | A282V | XP_006713557.1 |
| XM_011512417.1 | 1015 | Missense Mutation | GCG,GTG | A234V | XP_011510719.1 |