Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040160.2 | 784 | Silent Mutation | TCA,TCG | S147S | NP_001035250.1 |
NM_001040161.2 | 784 | Missense Mutation | CAG,CGG | Q73R | NP_001035251.1 |
NM_001040162.2 | 784 | Missense Mutation | CAG,CGG | Q93R | NP_001035252.1 |
NM_001040165.2 | 784 | Silent Mutation | TCA,TCG | S127S | NP_001035255.1 |
NM_001288710.1 | 784 | Missense Mutation | CAG,CGG | Q150R | NP_001275639.1 |
NM_032366.4 | 784 | Missense Mutation | CAG,CGG | Q170R | NP_115742.3 |
XM_011522713.2 | 784 | Missense Mutation | CAG,CGG | Q237R | XP_011521015.1 |
XM_011522714.2 | 784 | Missense Mutation | AGG,GGG | R179G | XP_011521016.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_053284.2 | 784 | Intron | NP_444514.1 |