Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207309.2 | 293 | Missense Mutation | GTG,TTG | V79L | NP_997192.2 |
XM_006717317.3 | 293 | Missense Mutation | GTG,TTG | V79L | XP_006717380.1 |
XM_011519182.2 | 293 | Intron | XP_011517484.1 |