ENST00000682424.1:c.1543T>C
|
ENSP00000507321.1:p.Phe515Leu
|
|
ENST00000299427.12:c.1657T>C
MANE Select
|
ENSP00000299427.6:p.Phe553Leu
|
|
ENST00000524611.2:n.696T>C
|
|
|
ENST00000533371.6:c.928T>C
|
ENSP00000437066.1:p.Phe310Leu
|
|
ENST00000642892.1:c.928T>C
|
ENSP00000494165.1:p.Phe310Leu
|
|
ENST00000643342.1:c.730T>C
|
|
|
ENST00000643439.1:c.*1397T>C
|
ENSP00000495849.1:n.*1397T>C
|
|
ENST00000643479.1:n.1843T>C
|
|
|
ENST00000643516.1:c.1166T>C
|
|
|
ENST00000644218.1:c.1468T>C
|
ENSP00000493574.1:p.Phe490Leu
|
|
ENST00000644683.1:c.*1110T>C
|
ENSP00000494085.1:n.*1110T>C
|
|
ENST00000644810.1:c.1378T>C
|
ENSP00000495895.1:p.Phe460Leu
|
|
ENST00000644831.1:n.1833T>C
|
|
|
ENST00000644933.1:c.*523T>C
|
ENSP00000496133.1:n.*523T>C
|
|
ENST00000645285.1:c.*523T>C
|
ENSP00000495058.1:n.*523T>C
|
|
ENST00000645331.1:n.2862T>C
|
|
|
ENST00000645620.1:c.928T>C
|
ENSP00000493657.1:p.Phe310Leu
|
|
ENST00000646691.1:n.1544T>C
|
|
|
ENST00000646777.1:n.1990T>C
|
|
|
ENST00000647016.1:n.2137T>C
|
|
|
ENST00000647152.1:c.928T>C
|
ENSP00000495893.1:p.Phe310Leu
|
|
ENST00000647209.1:c.*1526T>C
|
ENSP00000495558.1:n.*1526T>C
|
|
ENST00000647346.1:n.2677T>C
|
|
|
ENST00000299427.10:c.1657T>C
|
ENSP00000299427.6:p.Phe553Leu
|
|
ENST00000533371.5:c.928T>C
|
ENSP00000437066.1:p.Phe310Leu
|
|
ENST00000611494.4:c.1656T>C
|
ENSP00000484546.1:p.Thr552=
|
|
NM_000391.3:c.1657T>C
|
NP_000382.3:p.Phe553Leu
|
|
NM_000391.4:c.1657T>C
MANE Select
|
NP_000382.3:p.Phe553Leu
|
|