| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271779.1 | 1014 | Missense Mutation | GCG,GTG | A329V | NP_001258708.1 |
| NM_001271780.1 | 1014 | Missense Mutation | GCG,GTG | A238V | NP_001258709.1 |
| NM_001271781.1 | 1014 | Missense Mutation | GCG,GTG | A237V | NP_001258710.1 |
| NM_014814.2 | 1014 | Missense Mutation | GCG,GTG | A276V | NP_055629.1 |
| XM_005265619.1 | 1014 | Missense Mutation | GCG,GTG | A227V | XP_005265676.1 |
| XM_011534288.1 | 1014 | Intron | XP_011532590.1 | ||
| XM_017007569.1 | 1014 | Missense Mutation | GCG,GTG | A231V | XP_016863058.1 |