| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282629.1 | 1349 | UTR 3 | NP_001269558.1 | ||
| NM_001282632.1 | 1349 | Missense Mutation | CGC,TGC | R317C | NP_001269561.1 |
| NM_001288572.1 | 1349 | Missense Mutation | CGC,TGC | R287C | NP_001275501.1 |
| NM_001288573.1 | 1349 | Missense Mutation | CGC,TGC | R198C | NP_001275502.1 |
| NM_021996.5 | 1349 | Missense Mutation | CGC,TGC | R334C | NP_068836.2 |