Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138358.2 | 607 | Missense Mutation | CGG,TGG | R178W | NP_612367.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321439.1 | 607 | Intron | NP_001308368.1 | ||
NM_001321440.1 | 607 | Intron | NP_001308369.1 | ||
NM_024029.4 | 607 | Intron | NP_076934.1 | ||
XM_011528270.2 | 607 | Intron | XP_011526572.1 | ||
XM_011528271.2 | 607 | Intron | XP_011526573.1 |