| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286696.1 | 658 | Missense Mutation | GCT,GGT | A22G | NP_001273625.1 |
| NM_001286697.1 | 658 | Missense Mutation | GCT,GGT | A22G | NP_001273626.1 |
| NM_001286698.1 | 658 | Intron | NP_001273627.1 | ||
| NM_001322260.1 | 658 | Missense Mutation | GCT,GGT | A22G | NP_001309189.1 |
| NM_007135.2 | 658 | Missense Mutation | GCT,GGT | A46G | NP_009066.2 |
| XM_006717279.3 | 658 | Missense Mutation | GCT,GGT | A22G | XP_006717342.1 |