Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020737.2 | 3647 | Missense Mutation | CGG,TGG | R746W | NP_065788.1 |
XM_011514761.2 | 3647 | Missense Mutation | CGG,TGG | R746W | XP_011513063.1 |
XM_011514762.2 | 3647 | Missense Mutation | CGG,TGG | R746W | XP_011513064.1 |
XM_017011110.1 | 3647 | Missense Mutation | CGG,TGG | R746W | XP_016866599.1 |
XM_017011111.1 | 3647 | Intron | XP_016866600.1 |