| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001177701.2 | 855 | Missense Mutation | GCG,GTG | A142V | NP_001171172.1 |
| NM_006860.4 | 855 | Missense Mutation | GCG,GTG | A141V | NP_006851.1 |
| XM_006724106.2 | 855 | Missense Mutation | GCG,GTG | A142V | XP_006724169.1 |
| XM_017028540.1 | 855 | Missense Mutation | GCG,GTG | A101V | XP_016884029.1 |