| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152492.2 | 211 | Missense Mutation | CGC,TGC | R43C | NP_689705.2 |
| XM_011540780.1 | 211 | Missense Mutation | CGC,TGC | R43C | XP_011539082.1 |
| XM_017000402.1 | 211 | Missense Mutation | CGC,TGC | R43C | XP_016855891.1 |
| XM_017000403.1 | 211 | Missense Mutation | CGC,TGC | R43C | XP_016855892.1 |
| XM_017000404.1 | 211 | Missense Mutation | CGC,TGC | R43C | XP_016855893.1 |
| XM_017000405.1 | 211 | Missense Mutation | CGC,TGC | R43C | XP_016855894.1 |
| XM_017000406.1 | 211 | Intron | XP_016855895.1 |