Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136037.2 | 1029 | Missense Mutation | CAG,CGG | Q273R | NP_001129509.2 |
NM_001161403.1 | 1029 | Missense Mutation | CAG,CGG | Q251R | NP_001154875.1 |
NM_001161404.1 | 1029 | Missense Mutation | CAG,CGG | Q246R | NP_001154876.1 |
NM_001256542.1 | 1029 | Missense Mutation | CAG,CGG | Q99R | NP_001243471.1 |
NM_017980.4 | 1029 | Missense Mutation | CAG,CGG | Q275R | NP_060450.2 |
XM_005263710.2 | 1029 | Missense Mutation | CAG,CGG | Q182R | XP_005263767.1 |
XM_006712627.3 | 1029 | Missense Mutation | CAG,CGG | Q135R | XP_006712690.1 |
XM_006712628.3 | 1029 | Intron | XP_006712691.1 | ||
XM_011511453.1 | 1029 | Missense Mutation | AGC,GGC | S225G | XP_011509755.1 |
XM_017004469.1 | 1029 | Missense Mutation | AGC,GGC | S139G | XP_016859958.1 |