| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146202.1 | 1640 | Missense Mutation | CGC,TGC | R496C | NP_001139674.1 |
| NM_001146203.1 | 1640 | Missense Mutation | CGC,TGC | R418C | NP_001139675.1 |
| NM_001146204.1 | 1640 | Missense Mutation | CGC,TGC | R441C | NP_001139676.1 |
| NM_001146205.1 | 1640 | Missense Mutation | CGC,TGC | R476C | NP_001139677.1 |
| NM_001146206.1 | 1640 | Missense Mutation | CGC,TGC | R321C | NP_001139678.1 |
| NM_001146207.1 | 1640 | Missense Mutation | CGC,TGC | R413C | NP_001139679.1 |
| NM_170604.2 | 1640 | Missense Mutation | CGC,TGC | R510C | NP_733749.1 |