Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004620.3 | 1373 | Missense Mutation | ACG,ATG | T362M | NP_004611.1 |
NM_145803.2 | 1373 | Missense Mutation | ACG,ATG | T362M | NP_665802.1 |
XM_017018220.1 | 1373 | Intron | XP_016873709.1 |