|
ENST00000682424.1:c.517T>A
|
ENSP00000507321.1:p.Leu173Met
|
|
|
ENST00000299427.12:c.631T>A
MANE Select
|
ENSP00000299427.6:p.Leu211Met
|
|
|
ENST00000436873.7:c.312+270T>A
|
|
|
|
ENST00000524788.2:n.1790T>A
|
|
|
|
ENST00000524903.2:n.1906T>A
|
|
|
|
ENST00000528807.2:n.287T>A
|
|
|
|
ENST00000530040.2:n.479+328T>A
|
|
|
|
ENST00000533371.6:c.-99T>A
|
ENSP00000437066.1:n.-99T>A
|
|
|
ENST00000534644.6:n.579T>A
|
|
|
|
ENST00000642892.1:c.-99T>A
|
ENSP00000494165.1:n.-99T>A
|
|
|
ENST00000643439.1:c.*371T>A
|
ENSP00000495849.1:n.*371T>A
|
|
|
ENST00000643479.1:n.660T>A
|
|
|
|
ENST00000643516.1:c.395+270T>A
|
|
|
|
ENST00000644151.1:n.2070T>A
|
|
|
|
ENST00000644218.1:c.631T>A
|
ENSP00000493574.1:p.Leu211Met
|
|
|
ENST00000644683.1:c.*84T>A
|
ENSP00000494085.1:n.*84T>A
|
|
|
ENST00000644810.1:c.352T>A
|
ENSP00000495895.1:p.Leu118Met
|
|
|
ENST00000644831.1:n.807T>A
|
|
|
|
ENST00000644933.1:c.-99T>A
|
ENSP00000496133.1:n.-99T>A
|
|
|
ENST00000645020.1:n.1806T>A
|
|
|
|
ENST00000645285.1:c.-99T>A
|
ENSP00000495058.1:n.-99T>A
|
|
|
ENST00000645331.1:n.997T>A
|
|
|
|
ENST00000645620.1:c.-99T>A
|
ENSP00000493657.1:n.-99T>A
|
|
|
ENST00000646777.1:n.807T>A
|
|
|
|
ENST00000647016.1:n.1111T>A
|
|
|
|
ENST00000647152.1:c.-99T>A
|
ENSP00000495893.1:n.-99T>A
|
|
|
ENST00000647209.1:c.*500T>A
|
ENSP00000495558.1:n.*500T>A
|
|
|
ENST00000647346.1:n.1651T>A
|
|
|
|
ENST00000299427.10:c.631T>A
|
ENSP00000299427.6:p.Leu211Met
|
|
|
ENST00000428886.6:n.800T>A
|
|
|
|
ENST00000436873.6:c.450+328T>A
|
ENSP00000398136.2:n.450+328T>A
|
|
|
ENST00000524788.1:n.331T>A
|
|
|
|
ENST00000528571.5:c.*371T>A
|
ENSP00000434647.1:n.*371T>A
|
|
|
ENST00000528807.1:n.181T>A
|
|
|
|
ENST00000533371.5:c.-99T>A
|
ENSP00000437066.1:n.-99T>A
|
|
|
ENST00000534644.5:n.616T>A
|
|
|
|
ENST00000611494.4:c.631T>A
|
ENSP00000484546.1:p.Leu211Met
|
|
|
NM_000391.3:c.631T>A
|
NP_000382.3:p.Leu211Met
|
|
|
NM_000391.4:c.631T>A
MANE Select
|
NP_000382.3:p.Leu211Met
|
|
