Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318002.1 | 772 | Missense Mutation | CGT,TGT | R100C | NP_001304931.1 |
NM_173548.2 | 772 | Intron | NP_775819.1 | ||
XM_005258628.4 | 772 | Intron | XP_005258685.1 | ||
XM_005258630.4 | 772 | Missense Mutation | CGT,TGT | R108C | XP_005258687.1 |