Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006473.3 | 236 | Missense Mutation | ACG,ATG | T48M | NP_006464.1 |
XM_005273714.1 | 236 | Missense Mutation | ACG,ATG | T48M | XP_005273771.1 |
XM_017017100.1 | 236 | Intron | XP_016872589.1 |