ENST00000682424.1:c.1075T>G
|
ENSP00000507321.1:p.Phe359Val
|
|
ENST00000299427.12:c.1189T>G
MANE Select
|
ENSP00000299427.6:p.Phe397Val
|
|
ENST00000436873.7:c.426T>G
|
|
|
ENST00000524924.2:n.309T>G
|
|
|
ENST00000533371.6:c.460T>G
|
ENSP00000437066.1:p.Phe154Val
|
|
ENST00000642892.1:c.460T>G
|
ENSP00000494165.1:p.Phe154Val
|
|
ENST00000643342.1:c.262T>G
|
|
|
ENST00000643439.1:c.*929T>G
|
ENSP00000495849.1:n.*929T>G
|
|
ENST00000643479.1:n.1375T>G
|
|
|
ENST00000643516.1:c.698T>G
|
|
|
ENST00000644218.1:c.1000T>G
|
ENSP00000493574.1:p.Phe334Val
|
|
ENST00000644683.1:c.*642T>G
|
ENSP00000494085.1:n.*642T>G
|
|
ENST00000644810.1:c.910T>G
|
ENSP00000495895.1:p.Phe304Val
|
|
ENST00000644831.1:n.1365T>G
|
|
|
ENST00000644933.1:c.*55T>G
|
ENSP00000496133.1:n.*55T>G
|
|
ENST00000645285.1:c.*55T>G
|
ENSP00000495058.1:n.*55T>G
|
|
ENST00000645331.1:n.2394T>G
|
|
|
ENST00000645620.1:c.460T>G
|
ENSP00000493657.1:p.Phe154Val
|
|
ENST00000646691.1:n.964T>G
|
|
|
ENST00000646777.1:n.1522T>G
|
|
|
ENST00000647016.1:n.1669T>G
|
|
|
ENST00000647152.1:c.460T>G
|
ENSP00000495893.1:p.Phe154Val
|
|
ENST00000647209.1:c.*1058T>G
|
ENSP00000495558.1:n.*1058T>G
|
|
ENST00000647346.1:n.2209T>G
|
|
|
ENST00000299427.10:c.1189T>G
|
ENSP00000299427.6:p.Phe397Val
|
|
ENST00000524924.1:n.144T>G
|
|
|
ENST00000532191.1:n.242T>G
|
|
|
ENST00000533371.5:c.460T>G
|
ENSP00000437066.1:p.Phe154Val
|
|
ENST00000611494.4:c.1189T>G
|
ENSP00000484546.1:p.Phe397Val
|
|
NM_000391.3:c.1189T>G
|
NP_000382.3:p.Phe397Val
|
|
NM_000391.4:c.1189T>G
MANE Select
|
NP_000382.3:p.Phe397Val
|
|