Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321153.1 | 866 | Missense Mutation | CGG,CTG | R79L | NP_001308082.1 |
NM_007335.3 | 866 | Missense Mutation | CGG,CTG | R79L | NP_031361.2 |
NM_007337.3 | 866 | Missense Mutation | CGG,CTG | R79L | NP_031363.2 |
XM_006713438.3 | 866 | Missense Mutation | CGG,CTG | R79L | XP_006713501.1 |
XM_006713439.3 | 866 | Missense Mutation | CGG,CTG | R79L | XP_006713502.1 |
XM_006713440.3 | 866 | Missense Mutation | CGG,CTG | R79L | XP_006713503.1 |
XM_011534317.2 | 866 | Missense Mutation | CGG,CTG | R79L | XP_011532619.1 |
XM_011534318.2 | 866 | Missense Mutation | CGG,CTG | R79L | XP_011532620.1 |