Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267578.1 | 898 | Missense Mutation | ACG,ATG | T146M | NP_001254507.1 |
NM_015602.3 | 898 | Missense Mutation | ACG,ATG | T146M | NP_056417.2 |
XM_011509403.1 | 898 | Missense Mutation | ACG,ATG | T146M | XP_011507705.1 |
XM_011509404.1 | 898 | Missense Mutation | ACG,ATG | T146M | XP_011507706.1 |