| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014663.2 | 531 | Missense Mutation | CGC,TGC | R110C | NP_055478.2 |
| XM_005271354.3 | 531 | Missense Mutation | CGC,TGC | R110C | XP_005271411.1 |
| XM_005271355.3 | 531 | Missense Mutation | CGC,TGC | R110C | XP_005271412.1 |
| XM_005271356.3 | 531 | Missense Mutation | CGC,TGC | R19C | XP_005271413.1 |
| XM_011542467.2 | 531 | Intron | XP_011540769.2 | ||
| XM_017002912.1 | 531 | Missense Mutation | CGC,TGC | R19C | XP_016858401.1 |