ENST00000682424.1:c.1513G>T
|
ENSP00000507321.1:p.Asp505Tyr
|
|
ENST00000299427.12:c.1627G>T
MANE Select
|
ENSP00000299427.6:p.Asp543Tyr
|
|
ENST00000524611.2:n.666G>T
|
|
|
ENST00000524924.2:n.747G>T
|
|
|
ENST00000533371.6:c.898G>T
|
ENSP00000437066.1:p.Asp300Tyr
|
|
ENST00000642892.1:c.898G>T
|
ENSP00000494165.1:p.Asp300Tyr
|
|
ENST00000643342.1:c.700G>T
|
|
|
ENST00000643439.1:c.*1367G>T
|
ENSP00000495849.1:n.*1367G>T
|
|
ENST00000643479.1:n.1813G>T
|
|
|
ENST00000643516.1:c.1136G>T
|
|
|
ENST00000644218.1:c.1438G>T
|
ENSP00000493574.1:p.Asp480Tyr
|
|
ENST00000644683.1:c.*1080G>T
|
ENSP00000494085.1:n.*1080G>T
|
|
ENST00000644810.1:c.1348G>T
|
ENSP00000495895.1:p.Asp450Tyr
|
|
ENST00000644831.1:n.1803G>T
|
|
|
ENST00000644933.1:c.*493G>T
|
ENSP00000496133.1:n.*493G>T
|
|
ENST00000645285.1:c.*493G>T
|
ENSP00000495058.1:n.*493G>T
|
|
ENST00000645331.1:n.2832G>T
|
|
|
ENST00000645620.1:c.898G>T
|
ENSP00000493657.1:p.Asp300Tyr
|
|
ENST00000646691.1:n.1514G>T
|
|
|
ENST00000646777.1:n.1960G>T
|
|
|
ENST00000647016.1:n.2107G>T
|
|
|
ENST00000647152.1:c.898G>T
|
ENSP00000495893.1:p.Asp300Tyr
|
|
ENST00000647209.1:c.*1496G>T
|
ENSP00000495558.1:n.*1496G>T
|
|
ENST00000647346.1:n.2647G>T
|
|
|
ENST00000299427.10:c.1627G>T
|
ENSP00000299427.6:p.Asp543Tyr
|
|
ENST00000533371.5:c.898G>T
|
ENSP00000437066.1:p.Asp300Tyr
|
|
ENST00000611494.4:c.1627G>T
|
ENSP00000484546.1:p.Asp543Tyr
|
|
NM_000391.3:c.1627G>T
|
NP_000382.3:p.Asp543Tyr
|
|
NM_000391.4:c.1627G>T
MANE Select
|
NP_000382.3:p.Asp543Tyr
|
|