Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018000.2 | 598 | Missense Mutation | CAA,CGA | Q101R | NP_060470.2 |
XM_011511468.2 | 598 | Missense Mutation | CAA,CGA | Q151R | XP_011509770.1 |
XM_017004475.1 | 598 | Intron | XP_016859964.1 |