|
ENST00000682424.1:c.219C>G
|
ENSP00000507321.1:p.Cys73Trp
|
|
|
ENST00000299427.12:c.333C>G
MANE Select
|
ENSP00000299427.6:p.Cys111Trp
|
|
|
ENST00000428886.7:n.421C>G
|
|
|
|
ENST00000436873.7:c.137C>G
|
|
|
|
ENST00000524788.2:n.1345C>G
|
|
|
|
ENST00000524903.2:n.1461C>G
|
|
|
|
ENST00000528571.6:c.*73C>G
|
ENSP00000434647.1:n.*73C>G
|
|
|
ENST00000530040.2:n.362C>G
|
|
|
|
ENST00000533371.6:c.-397C>G
|
ENSP00000437066.1:n.-397C>G
|
|
|
ENST00000534644.6:n.334C>G
|
|
|
|
ENST00000642892.1:c.-344C>G
|
ENSP00000494165.1:n.-344C>G
|
|
|
ENST00000643439.1:c.*73C>G
|
ENSP00000495849.1:n.*73C>G
|
|
|
ENST00000643479.1:n.362C>G
|
|
|
|
ENST00000643516.1:c.220C>G
|
|
|
|
ENST00000644151.1:n.1625C>G
|
|
|
|
ENST00000644218.1:c.333C>G
|
ENSP00000493574.1:p.Cys111Trp
|
|
|
ENST00000644683.1:c.333C>G
|
ENSP00000494085.1:p.Cys111Trp
|
|
|
ENST00000644810.1:c.230-520C>G
|
ENSP00000495895.1:n.230-520C>G
|
|
|
ENST00000644831.1:n.362C>G
|
|
|
|
ENST00000644933.1:c.-397C>G
|
ENSP00000496133.1:n.-397C>G
|
|
|
ENST00000645020.1:n.1361C>G
|
|
|
|
ENST00000645285.1:c.-397C>G
|
ENSP00000495058.1:n.-397C>G
|
|
|
ENST00000645331.1:n.355C>G
|
|
|
|
ENST00000645620.1:c.-339C>G
|
ENSP00000493657.1:n.-339C>G
|
|
|
ENST00000646777.1:n.362C>G
|
|
|
|
ENST00000647016.1:n.666C>G
|
|
|
|
ENST00000647152.1:c.-397C>G
|
ENSP00000495893.1:n.-397C>G
|
|
|
ENST00000647209.1:c.*202C>G
|
ENSP00000495558.1:n.*202C>G
|
|
|
ENST00000647346.1:n.1353C>G
|
|
|
|
ENST00000299427.10:c.333C>G
|
ENSP00000299427.6:p.Cys111Trp
|
|
|
ENST00000428886.6:n.355C>G
|
|
|
|
ENST00000436873.6:c.333C>G
|
ENSP00000398136.2:p.Cys111Trp
|
|
|
ENST00000528571.5:c.*73C>G
|
ENSP00000434647.1:n.*73C>G
|
|
|
ENST00000530040.1:n.445C>G
|
|
|
|
ENST00000533371.5:c.-397C>G
|
ENSP00000437066.1:n.-397C>G
|
|
|
ENST00000534644.5:n.318C>G
|
|
|
|
ENST00000611494.4:c.333C>G
|
ENSP00000484546.1:p.Cys111Trp
|
|
|
NM_000391.3:c.333C>G
|
NP_000382.3:p.Cys111Trp
|
|
|
NM_000391.4:c.333C>G
MANE Select
|
NP_000382.3:p.Cys111Trp
|
|
