Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032880.4 | 417 | Missense Mutation | GGC,TGC | G12C | NP_116269.3 |
XM_011542319.2 | 417 | Missense Mutation | GGC,TGC | G12C | XP_011540621.1 |
XM_017002604.1 | 417 | Intron | XP_016858093.1 | ||
XM_017002605.1 | 417 | Intron | XP_016858094.1 |