| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032726.3 | 412 | Missense Mutation | CGC,TGC | R25C | NP_116115.1 |
| XM_005246913.2 | 412 | Missense Mutation | CGC,TGC | R25C | XP_005246970.1 |
| XM_011512012.1 | 412 | Missense Mutation | CGC,TGC | R25C | XP_011510314.1 |
| XM_017005114.1 | 412 | Missense Mutation | CGC,TGC | R25C | XP_016860603.1 |
| XM_017005115.1 | 412 | Missense Mutation | CGC,TGC | R25C | XP_016860604.1 |
| XM_017005116.1 | 412 | Missense Mutation | CGC,TGC | R25C | XP_016860605.1 |
| XM_017005117.1 | 412 | Missense Mutation | CGC,TGC | R25C | XP_016860606.1 |
| XM_017005118.1 | 412 | UTR 5 | XP_016860607.1 | ||
| XM_017005119.1 | 412 | Intron | XP_016860608.1 | ||
| XM_017005120.1 | 412 | Intron | XP_016860609.1 |