| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_139025.4 | 668 | Missense Mutation | GCT,GGT | A75G | NP_620594.1 |
| NM_139026.4 | 668 | Missense Mutation | GCT,GGT | A75G | NP_620595.1 |
| NM_139027.4 | 668 | Missense Mutation | GCT,GGT | A75G | NP_620596.2 |
| XM_011518176.2 | 668 | Intron | XP_011516478.1 | ||
| XM_011518178.1 | 668 | Intron | XP_011516480.1 | ||
| XM_011518179.1 | 668 | Intron | XP_011516481.1 | ||
| XM_017014232.1 | 668 | Missense Mutation | GCT,GGT | A71G | XP_016869721.1 |
| XM_017014233.1 | 668 | UTR 5 | XP_016869722.1 | ||
| XM_017014234.1 | 668 | Intron | XP_016869723.1 | ||
| XM_017014235.1 | 668 | Missense Mutation | GCT,GGT | A75G | XP_016869724.1 |