| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077710.2 | 1188 | Intron | NP_001071178.2 | ||
| XM_011510372.2 | 1188 | Intron | XP_011508674.1 | ||
| XM_017004689.1 | 1188 | Missense Mutation | GCG,GTG | A348V | XP_016860178.1 |
| XM_017004690.1 | 1188 | Missense Mutation | GCG,GTG | A348V | XP_016860179.1 |
| XM_017004691.1 | 1188 | Intron | XP_016860180.1 | ||
| XM_017004692.1 | 1188 | UTR 3 | XP_016860181.1 |