Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173039.2 | 659 | Missense Mutation | ACG,ATG | T107M | NP_766627.1 |
XM_005273917.4 | 659 | Missense Mutation | ACG,ATG | T107M | XP_005273974.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_017018644.1 | 659 | Intron | XP_016874133.1 |