| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164372.1 | 1332 | Missense Mutation | CGT,TGT | R305C | NP_001157844.1 |
| NM_001164373.1 | 1332 | Missense Mutation | CGT,TGT | R276C | NP_001157845.1 |
| NM_016301.3 | 1332 | Missense Mutation | CGT,TGT | R266C | NP_057385.3 |
| XM_005253896.4 | 1332 | Missense Mutation | CGT,TGT | R439C | XP_005253953.3 |
| XM_017019394.1 | 1332 | Missense Mutation | CGT,TGT | R244C | XP_016874883.1 |