| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001163321.2 | 409 | Missense Mutation | CGT,TGT | R66C | NP_001156793.2 |
| NM_001163322.2 | 409 | Missense Mutation | CGT,TGT | R19C | NP_001156794.1 |
| NM_001163323.2 | 409 | Missense Mutation | CGT,TGT | R19C | NP_001156795.1 |
| NM_001271835.1 | 409 | Missense Mutation | CGT,TGT | R31C | NP_001258764.1 |
| NM_001271836.1 | 409 | Missense Mutation | CGT,TGT | R31C | NP_001258765.1 |
| NM_033626.3 | 409 | Missense Mutation | CGT,TGT | R31C | NP_296375.1 |