| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252195.1 | 887 | Missense Mutation | GCG,GTG | A154V | NP_001239124.1 |
| NM_032596.3 | 887 | UTR 3 | NP_115985.2 | ||
| NM_147168.1 | 887 | UTR 3 | NP_671697.1 | ||
| NM_147169.2 | 887 | Missense Mutation | GCG,GTG | A101V | NP_671698.1 |
| XM_005251616.4 | 887 | Missense Mutation | GCG,GTG | A289V | XP_005251673.1 |
| XM_005251618.4 | 887 | Missense Mutation | GCG,GTG | A154V | XP_005251675.1 |
| XM_011518055.2 | 887 | Missense Mutation | GCG,GTG | A154V | XP_011516357.1 |