| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_023072.2 | 238 | Missense Mutation | CGT,TGT | R80C | NP_075560.2 |
| XM_005260023.3 | 238 | Missense Mutation | CGT,TGT | R80C | XP_005260080.1 |
| XM_017027153.1 | 238 | Missense Mutation | CGT,TGT | R80C | XP_016882642.1 |
| XM_017027154.1 | 238 | Missense Mutation | CGT,TGT | R80C | XP_016882643.1 |
| XM_017027155.1 | 238 | Missense Mutation | CGT,TGT | R80C | XP_016882644.1 |
| XM_017027156.1 | 238 | Intron | XP_016882645.1 | ||
| XM_017027157.1 | 238 | Missense Mutation | CGT,TGT | R80C | XP_016882646.1 |