ENST00000355808.10:c.688G>T
|
ENSP00000348062.6:p.Glu230Ter
|
|
ENST00000379805.4:c.*359G>T
|
ENSP00000369133.3:n.*359G>T
|
|
ENST00000417819.6:c.751G>T
|
ENSP00000404616.2:p.Glu251Ter
|
|
ENST00000423505.6:c.781G>T
|
ENSP00000406473.2:p.Glu261Ter
|
|
ENST00000481733.2:n.462G>T
|
|
|
ENST00000696704.1:c.482G>T
|
ENSP00000512823.1:p.Ter161Leu
|
|
ENST00000696705.1:c.*122G>T
|
ENSP00000512824.1:n.*122G>T
|
|
ENST00000422285.7:c.667G>T
MANE Select
|
ENSP00000394382.2:p.Glu223Ter
|
|
ENST00000379806.9:c.781G>T
|
ENSP00000369134.5:p.Glu261Ter
|
|
ENST00000422285.6:c.667G>T
|
ENSP00000394382.2:p.Glu223Ter
|
|
ENST00000479146.1:n.502G>T
|
|
|
ENST00000481733.1:n.95G>T
|
|
|
ENST00000540249.5:c.574G>T
|
ENSP00000440761.1:p.Glu192Ter
|
|
ENST00000545074.5:c.688G>T
|
ENSP00000438550.1:p.Glu230Ter
|
|
NM_000284.3:c.667G>T
|
NP_000275.1:p.Glu223Ter
|
|
NM_001173454.1:c.781G>T
|
NP_001166925.1:p.Glu261Ter
|
|
NM_001173455.1:c.688G>T
|
NP_001166926.1:p.Glu230Ter
|
|
NM_001173456.1:c.574G>T
|
NP_001166927.1:p.Glu192Ter
|
|
XM_011545531.1:c.802G>T
|
XP_011543833.1:p.Glu268Ter
|
|
XM_011545532.1:c.709G>T
|
XP_011543834.1:p.Glu237Ter
|
|
XM_017029574.2:c.688G>T
|
XP_016885063.1:p.Glu230Ter
|
|
NM_000284.4:c.667G>T
MANE Select
|
NP_000275.1:p.Glu223Ter
|
|
NM_001173454.2:c.781G>T
|
NP_001166925.1:p.Glu261Ter
|
|
NM_001173455.2:c.688G>T
|
NP_001166926.1:p.Glu230Ter
|
|
NM_001173456.2:c.574G>T
|
NP_001166927.1:p.Glu192Ter
|
|