Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174924.1 | 1092 | Missense Mutation | ATG,GTG | M562V | NP_777584.1 |
XM_011545764.1 | 1092 | Intron | XP_011544066.1 | ||
XM_011545765.1 | 1092 | Intron | XP_011544067.1 | ||
XM_011545766.2 | 1092 | Missense Mutation | ATG,GTG | M288V | XP_011544068.1 |