ENST00000682424.1:c.404T>A
|
ENSP00000507321.1:p.Leu135Gln
|
|
ENST00000299427.12:c.518T>A
MANE Select
|
ENSP00000299427.6:p.Leu173Gln
|
|
ENST00000428886.7:n.753T>A
|
|
|
ENST00000436873.7:c.312+157T>A
|
|
|
ENST00000524788.2:n.1677T>A
|
|
|
ENST00000524903.2:n.1793T>A
|
|
|
ENST00000528807.2:n.174T>A
|
|
|
ENST00000530040.2:n.479+215T>A
|
|
|
ENST00000533371.6:c.-212T>A
|
ENSP00000437066.1:n.-212T>A
|
|
ENST00000534644.6:n.466T>A
|
|
|
ENST00000642892.1:c.-212T>A
|
ENSP00000494165.1:n.-212T>A
|
|
ENST00000643439.1:c.*258T>A
|
ENSP00000495849.1:n.*258T>A
|
|
ENST00000643479.1:n.547T>A
|
|
|
ENST00000643516.1:c.395+157T>A
|
|
|
ENST00000644151.1:n.1957T>A
|
|
|
ENST00000644218.1:c.518T>A
|
ENSP00000493574.1:p.Leu173Gln
|
|
ENST00000644683.1:c.460T>A
|
ENSP00000494085.1:p.Cys154Ser
|
|
ENST00000644810.1:c.239T>A
|
ENSP00000495895.1:p.Leu80Gln
|
|
ENST00000644831.1:n.694T>A
|
|
|
ENST00000644933.1:c.-212T>A
|
ENSP00000496133.1:n.-212T>A
|
|
ENST00000645020.1:n.1693T>A
|
|
|
ENST00000645285.1:c.-212T>A
|
ENSP00000495058.1:n.-212T>A
|
|
ENST00000645331.1:n.884T>A
|
|
|
ENST00000645620.1:c.-212T>A
|
ENSP00000493657.1:n.-212T>A
|
|
ENST00000646777.1:n.694T>A
|
|
|
ENST00000647016.1:n.998T>A
|
|
|
ENST00000647152.1:c.-212T>A
|
ENSP00000495893.1:n.-212T>A
|
|
ENST00000647209.1:c.*387T>A
|
ENSP00000495558.1:n.*387T>A
|
|
ENST00000647346.1:n.1538T>A
|
|
|
ENST00000299427.10:c.518T>A
|
ENSP00000299427.6:p.Leu173Gln
|
|
ENST00000428886.6:n.687T>A
|
|
|
ENST00000436873.6:c.450+215T>A
|
ENSP00000398136.2:n.450+215T>A
|
|
ENST00000524788.1:n.218T>A
|
|
|
ENST00000528571.5:c.*258T>A
|
ENSP00000434647.1:n.*258T>A
|
|
ENST00000528807.1:n.68T>A
|
|
|
ENST00000533371.5:c.-212T>A
|
ENSP00000437066.1:n.-212T>A
|
|
ENST00000534644.5:n.503T>A
|
|
|
ENST00000611494.4:c.518T>A
|
ENSP00000484546.1:p.Leu173Gln
|
|
NM_000391.3:c.518T>A
|
NP_000382.3:p.Leu173Gln
|
|
NM_000391.4:c.518T>A
MANE Select
|
NP_000382.3:p.Leu173Gln
|
|