Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024756.2 | 2922 | Missense Mutation | GCT,GGT | A919G | NP_079032.2 |
XM_005270153.1 | 2922 | Missense Mutation | GCT,GGT | A858G | XP_005270210.1 |
XM_006717970.3 | 2922 | Missense Mutation | GCT,GGT | A858G | XP_006718033.1 |