Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278613.1 | 6167 | Intron | NP_001265542.1 | ||
NM_001278615.1 | 6167 | Intron | NP_001265544.1 | ||
NM_002587.4 | 6167 | Intron | NP_002578.2 | ||
NM_032420.3 | 6167 | Missense Mutation | ACG,ATG | T1230M | NP_115796.2 |
XM_005268452.2 | 6167 | Missense Mutation | ACG,ATG | T1274M | XP_005268509.1 |
XM_005268454.4 | 6167 | Intron | XP_005268511.1 | ||
XM_005268455.2 | 6167 | Missense Mutation | ACG,ATG | T851M | XP_005268512.1 |
XM_017009517.1 | 6167 | Missense Mutation | ACG,ATG | T851M | XP_016865006.1 |
XM_017009518.1 | 6167 | Intron | XP_016865007.1 |