| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152458.6 | 1100 | Missense Mutation | CGC,TGC | R212C | NP_689671.2 |
| XM_011545752.2 | 1100 | Missense Mutation | CGC,TGC | R225C | XP_011544054.1 |
| XM_011545753.2 | 1100 | Missense Mutation | CGC,TGC | R225C | XP_011544055.1 |
| XM_017022967.1 | 1100 | Missense Mutation | CGC,TGC | R212C | XP_016878456.1 |