Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001146726.1 | 995 | Missense Mutation | ACG,ATG | T313M | NP_001140198.1 |
NM_138379.2 | 995 | Missense Mutation | ACG,ATG | T341M | NP_612388.2 |
XM_011534694.2 | 995 | Intron | XP_011532996.1 | ||
XM_017010021.1 | 995 | Missense Mutation | ACG,ATG | T286M | XP_016865510.1 |