Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114108.1 | 1159 | Missense Mutation | CGG,TGG | R352W | NP_001107580.1 |
NM_017904.3 | 1159 | Intron | NP_060374.2 | ||
XM_011541671.2 | 1159 | Intron | XP_011539973.1 | ||
XM_017001582.1 | 1159 | Missense Mutation | CGG,TGG | R161W | XP_016857071.1 |