| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012444.2 | 211 | Missense Mutation | CGC,TGC | R40C | NP_036576.1 |
| NM_198265.1 | 211 | Missense Mutation | CGC,TGC | R40C | NP_937998.1 |
| XM_005260379.3 | 211 | Missense Mutation | CGC,TGC | R40C | XP_005260436.1 |
| XM_005260380.3 | 211 | Missense Mutation | CGC,TGC | R40C | XP_005260437.1 |
| XM_005260381.3 | 211 | Missense Mutation | CGC,TGC | R40C | XP_005260438.1 |
| XM_005260382.4 | 211 | Missense Mutation | CGC,TGC | R40C | XP_005260439.1 |
| XM_011528756.2 | 211 | Missense Mutation | CGC,TGC | R40C | XP_011527058.1 |
| XM_011528757.2 | 211 | Intron | XP_011527059.1 |