Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004766.2 | 2689 | Missense Mutation | ACA,CCA | T792P | NP_004757.1 |
XM_017007512.1 | 2689 | Missense Mutation | ACA,CCA | T763P | XP_016863001.1 |
XM_017007513.1 | 2689 | Missense Mutation | ACA,CCA | T538P | XP_016863002.1 |