Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001523.1 | 2368 | Missense Mutation | ATG,GTG | M472V | NP_001001523.1 |
NM_005060.3 | 2368 | Missense Mutation | ATG,GTG | M493V | NP_005051.2 |
XM_006711484.3 | 2368 | Missense Mutation | ATG,GTG | M626V | XP_006711547.2 |