| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014466.2 | 214 | Missense Mutation | CGC,TGC | R39C | NP_055281.2 |
| XM_005270753.2 | 214 | Missense Mutation | CGC,TGC | R39C | XP_005270810.1 |
| XM_011541258.2 | 214 | Missense Mutation | CGC,TGC | R39C | XP_011539560.1 |
| XM_017001055.1 | 214 | Missense Mutation | CGC,TGC | R39C | XP_016856544.1 |