Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016578.3 | 4089 | Missense Mutation | ACA,CCA | T1399P | NP_057662.3 |
XM_005274051.2 | 4089 | Missense Mutation | ACA,CCA | T1396P | XP_005274108.1 |
XM_017017923.1 | 4089 | Missense Mutation | ACA,CCA | T1358P | XP_016873412.1 |