Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152612.2 | 442 | Missense Mutation | CGT,TGT | R44C | NP_689825.2 |
XM_006724159.2 | 442 | Missense Mutation | CGT,TGT | R110C | XP_006724222.1 |
XM_011529984.2 | 442 | Missense Mutation | CGT,TGT | R9C | XP_011528286.1 |
XM_011529985.1 | 442 | Missense Mutation | CGT,TGT | R110C | XP_011528287.1 |