Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018110.3 | 1091 | Missense Mutation | CGC,TGC | R267C | NP_060580.2 |
XM_005256042.3 | 1091 | Missense Mutation | CGC,TGC | R267C | XP_005256099.1 |
XM_005256043.2 | 1091 | Missense Mutation | CGC,TGC | R267C | XP_005256100.1 |