ENST00000355808.10:c.870G>C
|
ENSP00000348062.6:p.Glu290Asp
|
|
ENST00000379805.4:c.*541G>C
|
ENSP00000369133.3:n.*541G>C
|
|
ENST00000417819.6:c.933G>C
|
ENSP00000404616.2:p.Glu311Asp
|
|
ENST00000423505.6:c.963G>C
|
ENSP00000406473.2:p.Glu321Asp
|
|
ENST00000481733.2:n.644G>C
|
|
|
ENST00000696704.1:c.*181G>C
|
ENSP00000512823.1:n.*181G>C
|
|
ENST00000696705.1:c.*304G>C
|
ENSP00000512824.1:n.*304G>C
|
|
ENST00000422285.7:c.849G>C
MANE Select
|
ENSP00000394382.2:p.Glu283Asp
|
|
ENST00000379804.1:c.6G>C
|
ENSP00000369132.1:p.Glu2Asp
|
|
ENST00000379806.9:c.963G>C
|
ENSP00000369134.5:p.Glu321Asp
|
|
ENST00000422285.6:c.849G>C
|
ENSP00000394382.2:p.Glu283Asp
|
|
ENST00000478795.1:n.288G>C
|
|
|
ENST00000481733.1:n.277G>C
|
|
|
ENST00000540249.5:c.756G>C
|
ENSP00000440761.1:p.Glu252Asp
|
|
ENST00000545074.5:c.870G>C
|
ENSP00000438550.1:p.Glu290Asp
|
|
NM_000284.3:c.849G>C
|
NP_000275.1:p.Glu283Asp
|
|
NM_001173454.1:c.963G>C
|
NP_001166925.1:p.Glu321Asp
|
|
NM_001173455.1:c.870G>C
|
NP_001166926.1:p.Glu290Asp
|
|
NM_001173456.1:c.756G>C
|
NP_001166927.1:p.Glu252Asp
|
|
XM_011545531.1:c.984G>C
|
XP_011543833.1:p.Glu328Asp
|
|
XM_011545532.1:c.891G>C
|
XP_011543834.1:p.Glu297Asp
|
|
XM_017029574.2:c.870G>C
|
XP_016885063.1:p.Glu290Asp
|
|
NM_000284.4:c.849G>C
MANE Select
|
NP_000275.1:p.Glu283Asp
|
|
NM_001173454.2:c.963G>C
|
NP_001166925.1:p.Glu321Asp
|
|
NM_001173455.2:c.870G>C
|
NP_001166926.1:p.Glu290Asp
|
|
NM_001173456.2:c.756G>C
|
NP_001166927.1:p.Glu252Asp
|
|