|
ENST00000682424.1:c.513C>G
|
ENSP00000507321.1:p.Tyr171Ter
|
|
|
ENST00000299427.12:c.627C>G
MANE Select
|
ENSP00000299427.6:p.Tyr209Ter
|
|
|
ENST00000436873.7:c.312+266C>G
|
|
|
|
ENST00000524788.2:n.1786C>G
|
|
|
|
ENST00000524903.2:n.1902C>G
|
|
|
|
ENST00000528807.2:n.283C>G
|
|
|
|
ENST00000530040.2:n.479+324C>G
|
|
|
|
ENST00000533371.6:c.-103C>G
|
ENSP00000437066.1:n.-103C>G
|
|
|
ENST00000534644.6:n.575C>G
|
|
|
|
ENST00000642892.1:c.-103C>G
|
ENSP00000494165.1:n.-103C>G
|
|
|
ENST00000643439.1:c.*367C>G
|
ENSP00000495849.1:n.*367C>G
|
|
|
ENST00000643479.1:n.656C>G
|
|
|
|
ENST00000643516.1:c.395+266C>G
|
|
|
|
ENST00000644151.1:n.2066C>G
|
|
|
|
ENST00000644218.1:c.627C>G
|
ENSP00000493574.1:p.Tyr209Ter
|
|
|
ENST00000644683.1:c.*80C>G
|
ENSP00000494085.1:n.*80C>G
|
|
|
ENST00000644810.1:c.348C>G
|
ENSP00000495895.1:p.Tyr116Ter
|
|
|
ENST00000644831.1:n.803C>G
|
|
|
|
ENST00000644933.1:c.-103C>G
|
ENSP00000496133.1:n.-103C>G
|
|
|
ENST00000645020.1:n.1802C>G
|
|
|
|
ENST00000645285.1:c.-103C>G
|
ENSP00000495058.1:n.-103C>G
|
|
|
ENST00000645331.1:n.993C>G
|
|
|
|
ENST00000645620.1:c.-103C>G
|
ENSP00000493657.1:n.-103C>G
|
|
|
ENST00000646777.1:n.803C>G
|
|
|
|
ENST00000647016.1:n.1107C>G
|
|
|
|
ENST00000647152.1:c.-103C>G
|
ENSP00000495893.1:n.-103C>G
|
|
|
ENST00000647209.1:c.*496C>G
|
ENSP00000495558.1:n.*496C>G
|
|
|
ENST00000647346.1:n.1647C>G
|
|
|
|
ENST00000299427.10:c.627C>G
|
ENSP00000299427.6:p.Tyr209Ter
|
|
|
ENST00000428886.6:n.796C>G
|
|
|
|
ENST00000436873.6:c.450+324C>G
|
ENSP00000398136.2:n.450+324C>G
|
|
|
ENST00000524788.1:n.327C>G
|
|
|
|
ENST00000528571.5:c.*367C>G
|
ENSP00000434647.1:n.*367C>G
|
|
|
ENST00000528807.1:n.177C>G
|
|
|
|
ENST00000533371.5:c.-103C>G
|
ENSP00000437066.1:n.-103C>G
|
|
|
ENST00000534644.5:n.612C>G
|
|
|
|
ENST00000611494.4:c.627C>G
|
ENSP00000484546.1:p.Tyr209Ter
|
|
|
NM_000391.3:c.627C>G
|
NP_000382.3:p.Tyr209Ter
|
|
|
NM_000391.4:c.627C>G
MANE Select
|
NP_000382.3:p.Tyr209Ter
|
|
