Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282424.2 | 186 | Intron | NP_001269353.1 | ||
NM_144670.5 | 186 | Missense Mutation | CGG,TGG | R30W | NP_653271.2 |
XM_011520566.2 | 186 | Missense Mutation | CGG,TGG | R30W | XP_011518868.1 |
XM_011520567.2 | 186 | Missense Mutation | CGG,TGG | R30W | XP_011518869.1 |
XM_017018868.1 | 186 | Missense Mutation | CGG,TGG | R30W | XP_016874357.1 |
XM_017018869.1 | 186 | Missense Mutation | CGG,TGG | R30W | XP_016874358.1 |
XM_017018870.1 | 186 | Missense Mutation | CGG,TGG | R30W | XP_016874359.1 |