Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008777.2 | 1379 | Missense Mutation | AAT,AGT | N426S | NP_001008777.2 |
XM_011524865.2 | 1379 | Missense Mutation | AAT,AGT | N400S | XP_011523167.1 |
XM_011524866.2 | 1379 | Missense Mutation | AAT,AGT | N369S | XP_011523168.1 |
XM_011524867.2 | 1379 | Intron | XP_011523169.1 |