ENST00000682424.1:c.412T>G
|
ENSP00000507321.1:p.Phe138Val
|
|
ENST00000299427.12:c.526T>G
MANE Select
|
ENSP00000299427.6:p.Phe176Val
|
|
ENST00000428886.7:n.761T>G
|
|
|
ENST00000436873.7:c.312+165T>G
|
|
|
ENST00000524788.2:n.1685T>G
|
|
|
ENST00000524903.2:n.1801T>G
|
|
|
ENST00000528807.2:n.182T>G
|
|
|
ENST00000530040.2:n.479+223T>G
|
|
|
ENST00000533371.6:c.-204T>G
|
ENSP00000437066.1:n.-204T>G
|
|
ENST00000534644.6:n.474T>G
|
|
|
ENST00000642892.1:c.-204T>G
|
ENSP00000494165.1:n.-204T>G
|
|
ENST00000643439.1:c.*266T>G
|
ENSP00000495849.1:n.*266T>G
|
|
ENST00000643479.1:n.555T>G
|
|
|
ENST00000643516.1:c.395+165T>G
|
|
|
ENST00000644151.1:n.1965T>G
|
|
|
ENST00000644218.1:c.526T>G
|
ENSP00000493574.1:p.Phe176Val
|
|
ENST00000644683.1:c.468T>G
|
ENSP00000494085.1:p.Val156=
|
|
ENST00000644810.1:c.247T>G
|
ENSP00000495895.1:p.Phe83Val
|
|
ENST00000644831.1:n.702T>G
|
|
|
ENST00000644933.1:c.-204T>G
|
ENSP00000496133.1:n.-204T>G
|
|
ENST00000645020.1:n.1701T>G
|
|
|
ENST00000645285.1:c.-204T>G
|
ENSP00000495058.1:n.-204T>G
|
|
ENST00000645331.1:n.892T>G
|
|
|
ENST00000645620.1:c.-204T>G
|
ENSP00000493657.1:n.-204T>G
|
|
ENST00000646777.1:n.702T>G
|
|
|
ENST00000647016.1:n.1006T>G
|
|
|
ENST00000647152.1:c.-204T>G
|
ENSP00000495893.1:n.-204T>G
|
|
ENST00000647209.1:c.*395T>G
|
ENSP00000495558.1:n.*395T>G
|
|
ENST00000647346.1:n.1546T>G
|
|
|
ENST00000299427.10:c.526T>G
|
ENSP00000299427.6:p.Phe176Val
|
|
ENST00000428886.6:n.695T>G
|
|
|
ENST00000436873.6:c.450+223T>G
|
ENSP00000398136.2:n.450+223T>G
|
|
ENST00000524788.1:n.226T>G
|
|
|
ENST00000528571.5:c.*266T>G
|
ENSP00000434647.1:n.*266T>G
|
|
ENST00000528807.1:n.76T>G
|
|
|
ENST00000533371.5:c.-204T>G
|
ENSP00000437066.1:n.-204T>G
|
|
ENST00000534644.5:n.511T>G
|
|
|
ENST00000611494.4:c.526T>G
|
ENSP00000484546.1:p.Phe176Val
|
|
NM_000391.3:c.526T>G
|
NP_000382.3:p.Phe176Val
|
|
NM_000391.4:c.526T>G
MANE Select
|
NP_000382.3:p.Phe176Val
|
|