ENST00000682424.1:c.180G>T
|
ENSP00000507321.1:p.Thr60=
|
|
ENST00000299427.12:c.294G>T
MANE Select
|
ENSP00000299427.6:p.Thr98=
|
|
ENST00000428886.7:n.382G>T
|
|
|
ENST00000436873.7:c.98G>T
|
|
|
ENST00000524788.2:n.1306G>T
|
|
|
ENST00000524903.2:n.1422G>T
|
|
|
ENST00000528571.6:c.*34G>T
|
ENSP00000434647.1:n.*34G>T
|
|
ENST00000530040.2:n.323G>T
|
|
|
ENST00000533371.6:c.-436G>T
|
ENSP00000437066.1:n.-436G>T
|
|
ENST00000534644.6:n.295G>T
|
|
|
ENST00000642892.1:c.-383G>T
|
ENSP00000494165.1:n.-383G>T
|
|
ENST00000643439.1:c.*34G>T
|
ENSP00000495849.1:n.*34G>T
|
|
ENST00000643479.1:n.323G>T
|
|
|
ENST00000643516.1:c.181G>T
|
|
|
ENST00000644151.1:n.1586G>T
|
|
|
ENST00000644218.1:c.294G>T
|
ENSP00000493574.1:p.Thr98=
|
|
ENST00000644683.1:c.294G>T
|
ENSP00000494085.1:p.Thr98=
|
|
ENST00000644810.1:c.230-559G>T
|
ENSP00000495895.1:n.230-559G>T
|
|
ENST00000644831.1:n.323G>T
|
|
|
ENST00000644933.1:c.-436G>T
|
ENSP00000496133.1:n.-436G>T
|
|
ENST00000645020.1:n.1322G>T
|
|
|
ENST00000645285.1:c.-436G>T
|
ENSP00000495058.1:n.-436G>T
|
|
ENST00000645331.1:n.316G>T
|
|
|
ENST00000645620.1:c.-378G>T
|
ENSP00000493657.1:n.-378G>T
|
|
ENST00000646777.1:n.323G>T
|
|
|
ENST00000647016.1:n.627G>T
|
|
|
ENST00000647152.1:c.-436G>T
|
ENSP00000495893.1:n.-436G>T
|
|
ENST00000647209.1:c.*163G>T
|
ENSP00000495558.1:n.*163G>T
|
|
ENST00000647346.1:n.1314G>T
|
|
|
ENST00000299427.10:c.294G>T
|
ENSP00000299427.6:p.Thr98=
|
|
ENST00000428886.6:n.316G>T
|
|
|
ENST00000436873.6:c.294G>T
|
ENSP00000398136.2:p.Thr98=
|
|
ENST00000528571.5:c.*34G>T
|
ENSP00000434647.1:n.*34G>T
|
|
ENST00000530040.1:n.406G>T
|
|
|
ENST00000533371.5:c.-436G>T
|
ENSP00000437066.1:n.-436G>T
|
|
ENST00000534644.5:n.279G>T
|
|
|
ENST00000611494.4:c.294G>T
|
ENSP00000484546.1:p.Thr98=
|
|
NM_000391.3:c.294G>T
|
NP_000382.3:p.Thr98=
|
|
NM_000391.4:c.294G>T
MANE Select
|
NP_000382.3:p.Thr98=
|
|