| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001113475.2 | 496 | Missense Mutation | GCG,GTG | A139V | NP_001106946.1 |
| XM_005267330.3 | 496 | Missense Mutation | GCG,GTG | A139V | XP_005267387.1 |
| XM_011536427.2 | 496 | Missense Mutation | GCG,GTG | A139V | XP_011534729.1 |
| XM_011536428.2 | 496 | Missense Mutation | GCG,GTG | A139V | XP_011534730.1 |
| XM_011536429.2 | 496 | Missense Mutation | GCG,GTG | A49V | XP_011534731.1 |
| XM_017020969.1 | 496 | Missense Mutation | GCG,GTG | A139V | XP_016876458.1 |
| XM_017020970.1 | 496 | Intron | XP_016876459.1 |