ENST00000355808.10:c.690G>T
|
ENSP00000348062.6:p.Glu230Asp
|
|
ENST00000379805.4:c.*361G>T
|
ENSP00000369133.3:n.*361G>T
|
|
ENST00000417819.6:c.753G>T
|
ENSP00000404616.2:p.Glu251Asp
|
|
ENST00000423505.6:c.783G>T
|
ENSP00000406473.2:p.Glu261Asp
|
|
ENST00000481733.2:n.464G>T
|
|
|
ENST00000696704.1:c.*1G>T
|
ENSP00000512823.1:n.*1G>T
|
|
ENST00000696705.1:c.*124G>T
|
ENSP00000512824.1:n.*124G>T
|
|
ENST00000422285.7:c.669G>T
MANE Select
|
ENSP00000394382.2:p.Glu223Asp
|
|
ENST00000379806.9:c.783G>T
|
ENSP00000369134.5:p.Glu261Asp
|
|
ENST00000422285.6:c.669G>T
|
ENSP00000394382.2:p.Glu223Asp
|
|
ENST00000479146.1:n.504G>T
|
|
|
ENST00000481733.1:n.97G>T
|
|
|
ENST00000540249.5:c.576G>T
|
ENSP00000440761.1:p.Glu192Asp
|
|
ENST00000545074.5:c.690G>T
|
ENSP00000438550.1:p.Glu230Asp
|
|
NM_000284.3:c.669G>T
|
NP_000275.1:p.Glu223Asp
|
|
NM_001173454.1:c.783G>T
|
NP_001166925.1:p.Glu261Asp
|
|
NM_001173455.1:c.690G>T
|
NP_001166926.1:p.Glu230Asp
|
|
NM_001173456.1:c.576G>T
|
NP_001166927.1:p.Glu192Asp
|
|
XM_011545531.1:c.804G>T
|
XP_011543833.1:p.Glu268Asp
|
|
XM_011545532.1:c.711G>T
|
XP_011543834.1:p.Glu237Asp
|
|
XM_017029574.2:c.690G>T
|
XP_016885063.1:p.Glu230Asp
|
|
NM_000284.4:c.669G>T
MANE Select
|
NP_000275.1:p.Glu223Asp
|
|
NM_001173454.2:c.783G>T
|
NP_001166925.1:p.Glu261Asp
|
|
NM_001173455.2:c.690G>T
|
NP_001166926.1:p.Glu230Asp
|
|
NM_001173456.2:c.576G>T
|
NP_001166927.1:p.Glu192Asp
|
|