Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001206957.1 | 607 | Missense Mutation | CGG,TGG | R39W | NP_001193886.1 |
NM_007182.4 | 607 | Missense Mutation | CGG,TGG | R190W | NP_009113.3 |
NM_170712.2 | 607 | Missense Mutation | CGG,TGG | R39W | NP_733830.1 |
NM_170713.2 | 607 | Missense Mutation | CGG,TGG | R120W | NP_733831.1 |
NM_170714.1 | 607 | Missense Mutation | CGG,TGG | R194W | NP_733832.1 |
XM_011533315.1 | 607 | Missense Mutation | CGG,TGG | R120W | XP_011531617.1 |
XM_011533316.2 | 607 | Missense Mutation | CGG,TGG | R39W | XP_011531618.1 |