Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173039.2 | 465 | Silent Mutation | CCA,CCG | P42P | NP_766627.1 |
XM_005273917.4 | 465 | Silent Mutation | CCA,CCG | P42P | XP_005273974.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_017018644.1 | 465 | Intron | XP_016874133.1 |