Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142605.1 | 288 | Intron | NP_001136077.1 | ||
NM_001258353.1 | 288 | Intron | NP_001245282.1 | ||
NM_001258354.1 | 288 | Intron | NP_001245283.1 | ||
NM_004247.3 | 288 | Intron | NP_004238.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271880.1 | 288 | Missense Mutation | CAG,CGG | Q48R | NP_001258809.1 |
NM_016438.3 | 288 | Missense Mutation | CAG,CGG | Q48R | NP_057522.1 |
XM_006721946.2 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_006722009.1 |
XM_006721947.3 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_006722010.1 |
XM_006721948.3 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_006722011.1 |
XM_011524891.2 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_011523193.1 |
XM_017024742.1 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_016880231.1 |
XM_017024743.1 | 288 | Missense Mutation | CAG,CGG | Q48R | XP_016880232.1 |