Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166356.1 | 557 | Missense Mutation | ATC,GTC | I150V | NP_001159828.1 |
NM_001166357.1 | 557 | Missense Mutation | ATC,GTC | I129V | NP_001159829.1 |
NM_001166358.1 | 557 | Missense Mutation | ATC,GTC | I129V | NP_001159830.1 |
NM_001166359.1 | 557 | Missense Mutation | ATC,GTC | I129V | NP_001159831.1 |
NM_005412.5 | 557 | Missense Mutation | ATC,GTC | I150V | NP_005403.2 |
XM_011538675.2 | 557 | Silent Mutation | CCA,CCG | P44P | XP_011536977.1 |
XM_011538676.2 | 557 | Silent Mutation | CCA,CCG | P44P | XP_011536978.1 |
XM_011538677.2 | 557 | Silent Mutation | CCA,CCG | P44P | XP_011536979.1 |
XM_011538678.2 | 557 | Silent Mutation | CCA,CCG | P44P | XP_011536980.1 |