Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001258290.1 | 2118 | Missense Mutation | CGG,TGG | R785W | NP_001245219.1 |
NM_001258291.1 | 2118 | Missense Mutation | CGG,TGG | R687W | NP_001245220.1 |
NM_173502.4 | 2118 | Missense Mutation | CGG,TGG | R790W | NP_775773.2 |
XM_011545758.2 | 2118 | Missense Mutation | CGG,TGG | R565W | XP_011544060.1 |
XM_017022968.1 | 2118 | Intron | XP_016878457.1 | ||
XM_017022969.1 | 2118 | Intron | XP_016878458.1 | ||
XM_017022970.1 | 2118 | UTR 3 | XP_016878459.1 | ||
XM_017022971.1 | 2118 | Missense Mutation | CCG,CTG | P613L | XP_016878460.1 |