| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002977.3 | 5947 | Missense Mutation | GCG,GTG | A1880V | NP_002968.1 |
| XM_005246757.2 | 5947 | Missense Mutation | GCG,GTG | A1891V | XP_005246814.1 |
| XM_011511616.2 | 5947 | Missense Mutation | GCG,GTG | A1891V | XP_011509918.1 |
| XM_011511617.2 | 5947 | Missense Mutation | GCG,GTG | A1891V | XP_011509919.1 |
| XM_011511618.2 | 5947 | Missense Mutation | GCG,GTG | A1880V | XP_011509920.1 |
| XM_011511619.2 | 5947 | Intron | XP_011509921.1 | ||
| XM_017004668.1 | 5947 | Missense Mutation | GCG,GTG | A1762V | XP_016860157.1 |
| XM_017004669.1 | 5947 | Missense Mutation | GCG,GTG | A1643V | XP_016860158.1 |