Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002250.2 | 1589 | Missense Mutation | ACG,ATG | T398M | NP_002241.1 |
XM_005258882.2 | 1589 | Missense Mutation | ACG,ATG | T366M | XP_005258939.1 |
XM_005258883.2 | 1589 | Missense Mutation | ACG,ATG | T335M | XP_005258940.1 |
XM_011526938.1 | 1589 | Intron | XP_011525240.1 |