Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297763.1 | 292 | Intron | NP_001284692.1 | ||
NM_178544.4 | 292 | Missense Mutation | AAA,AAT | K12N | NP_848639.2 |
XM_011526898.2 | 292 | Intron | XP_011525200.1 | ||
XM_011526899.2 | 292 | Missense Mutation | AAA,AAT | K12N | XP_011525201.1 |