Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_130767.2 | 1287 | Intron | NP_570123.1 | ||
XM_006714531.2 | 1287 | Intron | XP_006714594.1 | ||
XM_006714532.3 | 1287 | Intron | XP_006714595.1 | ||
XM_017009045.1 | 1287 | Intron | XP_016864534.1 | ||
XM_017009046.1 | 1287 | Intron | XP_016864535.1 | ||
XM_017009047.1 | 1287 | Intron | XP_016864536.1 | ||
XM_017009048.1 | 1287 | Intron | XP_016864537.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001131035.1 | 1287 | Missense Mutation | CCT,CTT | P266L | NP_001124507.1 |
NM_001131036.1 | 1287 | Missense Mutation | CCT,CTT | P266L | NP_001124508.1 |
NM_032280.2 | 1287 | Missense Mutation | CCT,CTT | P266L | NP_115656.1 |
XM_005248616.3 | 1287 | Missense Mutation | CCT,CTT | P115L | XP_005248673.1 |