Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099646.1 | 1700 | Missense Mutation | AAG,CAG | K473Q | NP_001093116.1 |
NM_001256663.1 | 1700 | Missense Mutation | AAG,CAG | K487Q | NP_001243592.1 |
NM_152908.3 | 1700 | Missense Mutation | AAG,CAG | K509Q | NP_690872.2 |
XM_017024221.1 | 1700 | Missense Mutation | AAG,CAG | K523Q | XP_016879710.1 |
XM_017024222.1 | 1700 | Missense Mutation | AAG,CAG | K474Q | XP_016879711.1 |
XM_017024223.1 | 1700 | Intron | XP_016879712.1 | ||
XM_017024224.1 | 1700 | Intron | XP_016879713.1 | ||
XM_017024225.1 | 1700 | Intron | XP_016879714.1 | ||
XM_017024226.1 | 1700 | Intron | XP_016879715.1 |