| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012991.2 | 1433 | Intron | NP_001013009.2 | ||
| XM_005255317.4 | 1433 | Intron | XP_005255374.1 | ||
| XM_006721046.3 | 1433 | Missense Mutation | CGC,TGC | R392C | XP_006721109.1 |
| XM_011545855.1 | 1433 | Missense Mutation | CGC,TGC | R452C | XP_011544157.1 |
| XM_017023231.1 | 1433 | Intron | XP_016878720.1 | ||
| XM_017023232.1 | 1433 | Missense Mutation | CGC,TGC | R369C | XP_016878721.1 |