Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153698.1 | 689 | Missense Mutation | ACA,ATA | T218I | NP_714542.1 |
XM_005251783.3 | 689 | Missense Mutation | ACA,ATA | T174I | XP_005251840.1 |
XM_005251784.4 | 689 | Intron | XP_005251841.1 |