Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077663.2 | 2824 | Missense Mutation | ATG,CTG | M779L | NP_001071131.1 |
NM_001077664.2 | 2824 | Missense Mutation | ATG,CTG | M736L | NP_001071132.1 |
NM_001290075.1 | 2824 | Missense Mutation | ATG,CTG | M736L | NP_001277004.1 |
NM_001290076.1 | 2824 | Missense Mutation | ATG,CTG | M736L | NP_001277005.1 |
NM_017920.4 | 2824 | Missense Mutation | ATG,CTG | M770L | NP_060390.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204871.1 | 2824 | Intron | NP_001191800.1 |