Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001083590.1 | 291 | Missense Mutation | CGG,TGG | R70W | NP_001077059.1 |
NM_017727.4 | 291 | Missense Mutation | CGG,TGG | R70W | NP_060197.4 |
XM_005264381.3 | 291 | Missense Mutation | CGG,TGG | R70W | XP_005264438.1 |
XM_005264382.3 | 291 | Missense Mutation | CGG,TGG | R70W | XP_005264439.1 |
XM_005264383.3 | 291 | Intron | XP_005264440.1 |