| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153357.1 | 1416 | Missense Mutation | GCG,GTG | A282V | NP_699188.1 |
| XM_005256488.3 | 1416 | Missense Mutation | GCG,GTG | A377V | XP_005256545.2 |
| XM_017024281.1 | 1416 | Missense Mutation | GCG,GTG | A377V | XP_016879770.1 |
| XM_017024282.1 | 1416 | Intron | XP_016879771.1 |