| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000895.2 | 1860 | Missense Mutation | GCG,GTG | A604V | NP_000886.1 |
| NM_001256643.1 | 1860 | Missense Mutation | GCG,GTG | A580V | NP_001243572.1 |
| NM_001256644.1 | 1860 | UTR 3 | NP_001243573.1 | ||
| XM_005268871.1 | 1860 | UTR 3 | XP_005268928.1 | ||
| XM_011538348.1 | 1860 | Intron | XP_011536650.1 | ||
| XM_011538349.2 | 1860 | Intron | XP_011536651.1 |