| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282629.1 | 1256 | UTR 3 | NP_001269558.1 | ||
| NM_001282632.1 | 1256 | Missense Mutation | CGT,TGT | R286C | NP_001269561.1 |
| NM_001288572.1 | 1256 | Missense Mutation | CGT,TGT | R256C | NP_001275501.1 |
| NM_001288573.1 | 1256 | Missense Mutation | CGT,TGT | R167C | NP_001275502.1 |
| NM_021996.5 | 1256 | Missense Mutation | CGT,TGT | R303C | NP_068836.2 |