Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000851.3 | 656 | Missense Mutation | CGC,TGC | R187C | NP_000842.2 |
XM_005270784.4 | 656 | Missense Mutation | CGC,TGC | R187C | XP_005270841.1 |
XM_005270785.4 | 656 | Missense Mutation | CGC,TGC | R83C | XP_005270842.1 |