Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002583.2 | 1061 | Missense Mutation | ATG,GTG | M299V | NP_002574.2 |
XM_006719435.2 | 1061 | Missense Mutation | ATG,GTG | M299V | XP_006719498.1 |
XM_006719436.3 | 1061 | Intron | XP_006719499.1 | ||
XM_017019377.1 | 1061 | Missense Mutation | ATG,GTG | M299V | XP_016874866.1 |
XM_017019378.1 | 1061 | Intron | XP_016874867.1 | ||
XM_017019379.1 | 1061 | Intron | XP_016874868.1 |