Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001200029.1 | 1219 | Missense Mutation | ATG,GTG | M316V | NP_001186958.1 |
NM_001200030.1 | 1219 | Intron | NP_001186959.1 | ||
NM_001200031.1 | 1219 | Missense Mutation | ATG,GTG | M67V | NP_001186960.1 |
NM_001200032.1 | 1219 | Intron | NP_001186961.1 | ||
NM_003549.3 | 1219 | Missense Mutation | ATG,GTG | M316V | NP_003540.2 |