|
ENST00000682424.1:c.229A>G
|
ENSP00000507321.1:p.Ile77Val
|
|
|
ENST00000299427.12:c.343A>G
MANE Select
|
ENSP00000299427.6:p.Ile115Val
|
|
|
ENST00000428886.7:n.431A>G
|
|
|
|
ENST00000436873.7:c.147A>G
|
|
|
|
ENST00000524788.2:n.1355A>G
|
|
|
|
ENST00000524903.2:n.1471A>G
|
|
|
|
ENST00000528571.6:c.*83A>G
|
ENSP00000434647.1:n.*83A>G
|
|
|
ENST00000530040.2:n.372A>G
|
|
|
|
ENST00000533371.6:c.-387A>G
|
ENSP00000437066.1:n.-387A>G
|
|
|
ENST00000534644.6:n.344A>G
|
|
|
|
ENST00000642892.1:c.-334A>G
|
ENSP00000494165.1:n.-334A>G
|
|
|
ENST00000643439.1:c.*83A>G
|
ENSP00000495849.1:n.*83A>G
|
|
|
ENST00000643479.1:n.372A>G
|
|
|
|
ENST00000643516.1:c.230A>G
|
|
|
|
ENST00000644151.1:n.1635A>G
|
|
|
|
ENST00000644218.1:c.343A>G
|
ENSP00000493574.1:p.Ile115Val
|
|
|
ENST00000644683.1:c.343A>G
|
ENSP00000494085.1:p.Ile115Val
|
|
|
ENST00000644810.1:c.230-510A>G
|
ENSP00000495895.1:n.230-510A>G
|
|
|
ENST00000644831.1:n.372A>G
|
|
|
|
ENST00000644933.1:c.-387A>G
|
ENSP00000496133.1:n.-387A>G
|
|
|
ENST00000645020.1:n.1371A>G
|
|
|
|
ENST00000645285.1:c.-387A>G
|
ENSP00000495058.1:n.-387A>G
|
|
|
ENST00000645331.1:n.365A>G
|
|
|
|
ENST00000645620.1:c.-329A>G
|
ENSP00000493657.1:n.-329A>G
|
|
|
ENST00000646777.1:n.372A>G
|
|
|
|
ENST00000647016.1:n.676A>G
|
|
|
|
ENST00000647152.1:c.-387A>G
|
ENSP00000495893.1:n.-387A>G
|
|
|
ENST00000647209.1:c.*212A>G
|
ENSP00000495558.1:n.*212A>G
|
|
|
ENST00000647346.1:n.1363A>G
|
|
|
|
ENST00000299427.10:c.343A>G
|
ENSP00000299427.6:p.Ile115Val
|
|
|
ENST00000428886.6:n.365A>G
|
|
|
|
ENST00000436873.6:c.343A>G
|
ENSP00000398136.2:p.Ile115Val
|
|
|
ENST00000528571.5:c.*83A>G
|
ENSP00000434647.1:n.*83A>G
|
|
|
ENST00000530040.1:n.455A>G
|
|
|
|
ENST00000533371.5:c.-387A>G
|
ENSP00000437066.1:n.-387A>G
|
|
|
ENST00000534644.5:n.328A>G
|
|
|
|
ENST00000611494.4:c.343A>G
|
ENSP00000484546.1:p.Ile115Val
|
|
|
NM_000391.3:c.343A>G
|
NP_000382.3:p.Ile115Val
|
|
|
NM_000391.4:c.343A>G
MANE Select
|
NP_000382.3:p.Ile115Val
|
|
