Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042693.2 | 199 | Missense Mutation | CGC,GGC | R17G | NP_001036158.1 |
XM_011541377.2 | 199 | Intron | XP_011539679.1 | ||
XM_011541378.2 | 199 | Intron | XP_011539680.1 |