Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152353.2 | 1255 | Silent Mutation | TGC,TGT | C65C | NP_689566.1 |
XM_011526425.2 | 1255 | Silent Mutation | TGC,TGT | C65C | XP_011524727.1 |
XM_011526428.2 | 1255 | Silent Mutation | TGC,TGT | C65C | XP_011524730.1 |
XM_017026244.1 | 1255 | Missense Mutation | CAT,TAT | H193Y | XP_016881733.1 |
XM_017026245.1 | 1255 | Missense Mutation | CAT,TAT | H193Y | XP_016881734.1 |
XM_017026246.1 | 1255 | Silent Mutation | TGC,TGT | C65C | XP_016881735.1 |
XM_017026247.1 | 1255 | Missense Mutation | CAT,TAT | H193Y | XP_016881736.1 |