Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164232.1 | 1047 | Intron | NP_001157704.1 | ||
NM_001164234.1 | 1047 | Intron | NP_001157706.1 | ||
NM_015214.2 | 1047 | Intron | NP_056029.2 | ||
XM_005273454.2 | 1047 | Intron | XP_005273511.1 | ||
XM_005273455.3 | 1047 | Intron | XP_005273512.1 | ||
XM_005273456.3 | 1047 | Intron | XP_005273513.1 | ||
XM_011544456.1 | 1047 | Intron | XP_011542758.1 | ||
XM_017013252.1 | 1047 | Intron | XP_016868741.1 | ||
XM_017013253.1 | 1047 | Intron | XP_016868742.1 | ||
XM_017013254.1 | 1047 | Intron | XP_016868743.1 | ||
XM_017013255.1 | 1047 | Intron | XP_016868744.1 | ||
XM_017013256.1 | 1047 | Intron | XP_016868745.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001102559.1 | 1047 | Missense Mutation | CAG,CGG | Q229R | NP_001096029.1 |
NM_001102560.1 | 1047 | Intron | NP_001096030.1 | ||
NM_032483.3 | 1047 | Intron | NP_115872.2 | ||
XM_005273661.4 | 1047 | Intron | XP_005273718.2 | ||
XM_005273663.3 | 1047 | Intron | XP_005273720.2 | ||
XM_011544670.2 | 1047 | Intron | XP_011542972.1 | ||
XM_011544671.1 | 1047 | Missense Mutation | CAG,CGG | Q188R | XP_011542973.1 |
XM_011544672.1 | 1047 | Missense Mutation | CAG,CGG | Q172R | XP_011542974.1 |
XM_011544674.2 | 1047 | Intron | XP_011542976.1 | ||
XM_011544675.2 | 1047 | Intron | XP_011542977.1 | ||
XM_017013905.1 | 1047 | Intron | XP_016869394.1 | ||
XM_017013906.1 | 1047 | Intron | XP_016869395.1 | ||
XM_017013907.1 | 1047 | Intron | XP_016869396.1 |