Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006851.2 | 137 | Missense Mutation | ACA,GCA | T4A | NP_006842.2 |
XM_011537775.2 | 137 | Missense Mutation | ACA,GCA | T4A | XP_011536077.1 |
XM_017018721.1 | 137 | Intron | XP_016874210.1 |