Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318202.1 | 3866 | Missense Mutation | ATG,CTG | M1180L | NP_001305131.1 |
NM_013241.2 | 3866 | Missense Mutation | ATG,CTG | M1154L | NP_037373.2 |
XM_006721180.1 | 3866 | Missense Mutation | ATG,CTG | M685L | XP_006721243.1 |
XM_011523043.2 | 3866 | Missense Mutation | ATG,CTG | M1170L | XP_011521345.1 |
XM_011523044.1 | 3866 | Missense Mutation | ATG,CTG | M1126L | XP_011521346.1 |
XM_011523045.2 | 3866 | Missense Mutation | ATG,CTG | M1087L | XP_011521347.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318217.1 | 3866 | Intron | NP_001305146.1 | ||
NM_014187.3 | 3866 | Intron | NP_054906.2 |