| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001198559.1 | 788 | UTR 3 | NP_001185488.1 | ||
| NM_016544.2 | 788 | Missense Mutation | GCG,GTG | A236V | NP_057628.1 |
| XM_011532902.1 | 788 | Intron | XP_011531204.1 | ||
| XM_017004269.1 | 788 | Missense Mutation | GCG,GTG | A165V | XP_016859758.1 |
| XM_017004270.1 | 788 | Missense Mutation | GCG,GTG | A165V | XP_016859759.1 |