Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020661.2 | 614 | Missense Mutation | NP_065712.1 | ||
XM_011520772.2 | 614 | Missense Mutation | ACG,ATG | T139M | XP_011519074.1 |
XM_011520773.2 | 614 | Missense Mutation | ACG,ATG | T139M | XP_011519075.1 |