| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040647.1 | 171 | Missense Mutation | GCG,GTG | A9V | NP_001035737.1 |
| NM_001040648.1 | 171 | Intron | NP_001035738.1 | ||
| NM_001142414.1 | 171 | Missense Mutation | GCG,GTG | A35V | NP_001135886.1 |
| NM_014478.4 | 171 | Missense Mutation | GCG,GTG | A9V | NP_055293.1 |