ENST00000682424.1:c.574T>G
|
ENSP00000507321.1:p.Phe192Val
|
|
ENST00000299427.12:c.688T>G
MANE Select
|
ENSP00000299427.6:p.Phe230Val
|
|
ENST00000436873.7:c.312+442T>G
|
|
|
ENST00000524788.2:n.1847T>G
|
|
|
ENST00000524903.2:n.1963T>G
|
|
|
ENST00000528807.2:n.344T>G
|
|
|
ENST00000530040.2:n.480-356T>G
|
|
|
ENST00000533371.6:c.-42T>G
|
ENSP00000437066.1:n.-42T>G
|
|
ENST00000642892.1:c.-42T>G
|
ENSP00000494165.1:n.-42T>G
|
|
ENST00000643439.1:c.*428T>G
|
ENSP00000495849.1:n.*428T>G
|
|
ENST00000643479.1:n.717T>G
|
|
|
ENST00000643516.1:c.396-356T>G
|
|
|
ENST00000644151.1:n.2127T>G
|
|
|
ENST00000644218.1:c.688T>G
|
ENSP00000493574.1:p.Phe230Val
|
|
ENST00000644683.1:c.*141T>G
|
ENSP00000494085.1:n.*141T>G
|
|
ENST00000644810.1:c.409T>G
|
ENSP00000495895.1:p.Phe137Val
|
|
ENST00000644831.1:n.864T>G
|
|
|
ENST00000644933.1:c.-42T>G
|
ENSP00000496133.1:n.-42T>G
|
|
ENST00000645020.1:n.1978T>G
|
|
|
ENST00000645285.1:c.-42T>G
|
ENSP00000495058.1:n.-42T>G
|
|
ENST00000645331.1:n.1054T>G
|
|
|
ENST00000645620.1:c.-42T>G
|
ENSP00000493657.1:n.-42T>G
|
|
ENST00000646777.1:n.864T>G
|
|
|
ENST00000647016.1:n.1168T>G
|
|
|
ENST00000647152.1:c.-42T>G
|
ENSP00000495893.1:n.-42T>G
|
|
ENST00000647209.1:c.*557T>G
|
ENSP00000495558.1:n.*557T>G
|
|
ENST00000647346.1:n.1708T>G
|
|
|
ENST00000299427.10:c.688T>G
|
ENSP00000299427.6:p.Phe230Val
|
|
ENST00000436873.6:c.451-356T>G
|
ENSP00000398136.2:n.451-356T>G
|
|
ENST00000524788.1:n.388T>G
|
|
|
ENST00000528807.1:n.238T>G
|
|
|
ENST00000533371.5:c.-42T>G
|
ENSP00000437066.1:n.-42T>G
|
|
ENST00000611494.4:c.688T>G
|
ENSP00000484546.1:p.Phe230Val
|
|
NM_000391.3:c.688T>G
|
NP_000382.3:p.Phe230Val
|
|
NM_000391.4:c.688T>G
MANE Select
|
NP_000382.3:p.Phe230Val
|
|