| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_207395.2 | 294 | Missense Mutation | CGT,TGT | R55C | NP_997278.2 |
| XM_005258915.4 | 294 | Missense Mutation | CGT,TGT | R55C | XP_005258972.1 |
| XM_005258918.4 | 294 | Missense Mutation | CGT,TGT | R55C | XP_005258975.1 |