Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000958.2 | 1235 | Missense Mutation | CGC,TGC | R215C | NP_000949.1 |
XM_017009656.1 | 1235 | Missense Mutation | CGC,TGC | R215C | XP_016865145.1 |
XM_017009657.1 | 1235 | Missense Mutation | CGC,TGC | R215C | XP_016865146.1 |
XM_017009658.1 | 1235 | Missense Mutation | CGC,TGC | R215C | XP_016865147.1 |
XM_017009659.1 | 1235 | Missense Mutation | CGC,TGC | R215C | XP_016865148.1 |