|
ENST00000682424.1:c.232A>G
|
ENSP00000507321.1:p.Thr78Ala
|
|
|
ENST00000299427.12:c.346A>G
MANE Select
|
ENSP00000299427.6:p.Thr116Ala
|
|
|
ENST00000428886.7:n.434A>G
|
|
|
|
ENST00000436873.7:c.150A>G
|
|
|
|
ENST00000524788.2:n.1358A>G
|
|
|
|
ENST00000524903.2:n.1474A>G
|
|
|
|
ENST00000528571.6:c.*86A>G
|
ENSP00000434647.1:n.*86A>G
|
|
|
ENST00000530040.2:n.375A>G
|
|
|
|
ENST00000533371.6:c.-384A>G
|
ENSP00000437066.1:n.-384A>G
|
|
|
ENST00000534644.6:n.347A>G
|
|
|
|
ENST00000642892.1:c.-331A>G
|
ENSP00000494165.1:n.-331A>G
|
|
|
ENST00000643439.1:c.*86A>G
|
ENSP00000495849.1:n.*86A>G
|
|
|
ENST00000643479.1:n.375A>G
|
|
|
|
ENST00000643516.1:c.233A>G
|
|
|
|
ENST00000644151.1:n.1638A>G
|
|
|
|
ENST00000644218.1:c.346A>G
|
ENSP00000493574.1:p.Thr116Ala
|
|
|
ENST00000644683.1:c.346A>G
|
ENSP00000494085.1:p.Thr116Ala
|
|
|
ENST00000644810.1:c.230-507A>G
|
ENSP00000495895.1:n.230-507A>G
|
|
|
ENST00000644831.1:n.375A>G
|
|
|
|
ENST00000644933.1:c.-384A>G
|
ENSP00000496133.1:n.-384A>G
|
|
|
ENST00000645020.1:n.1374A>G
|
|
|
|
ENST00000645285.1:c.-384A>G
|
ENSP00000495058.1:n.-384A>G
|
|
|
ENST00000645331.1:n.368A>G
|
|
|
|
ENST00000645620.1:c.-326A>G
|
ENSP00000493657.1:n.-326A>G
|
|
|
ENST00000646777.1:n.375A>G
|
|
|
|
ENST00000647016.1:n.679A>G
|
|
|
|
ENST00000647152.1:c.-384A>G
|
ENSP00000495893.1:n.-384A>G
|
|
|
ENST00000647209.1:c.*215A>G
|
ENSP00000495558.1:n.*215A>G
|
|
|
ENST00000647346.1:n.1366A>G
|
|
|
|
ENST00000299427.10:c.346A>G
|
ENSP00000299427.6:p.Thr116Ala
|
|
|
ENST00000428886.6:n.368A>G
|
|
|
|
ENST00000436873.6:c.346A>G
|
ENSP00000398136.2:p.Thr116Ala
|
|
|
ENST00000528571.5:c.*86A>G
|
ENSP00000434647.1:n.*86A>G
|
|
|
ENST00000530040.1:n.458A>G
|
|
|
|
ENST00000533371.5:c.-384A>G
|
ENSP00000437066.1:n.-384A>G
|
|
|
ENST00000534644.5:n.331A>G
|
|
|
|
ENST00000611494.4:c.346A>G
|
ENSP00000484546.1:p.Thr116Ala
|
|
|
NM_000391.3:c.346A>G
|
NP_000382.3:p.Thr116Ala
|
|
|
NM_000391.4:c.346A>G
MANE Select
|
NP_000382.3:p.Thr116Ala
|
|
