ENST00000682424.1:c.448C>T
|
ENSP00000507321.1:p.Pro150Ser
|
|
ENST00000299427.12:c.562C>T
MANE Select
|
ENSP00000299427.6:p.Pro188Ser
|
|
ENST00000428886.7:n.797C>T
|
|
|
ENST00000436873.7:c.312+201C>T
|
|
|
ENST00000524788.2:n.1721C>T
|
|
|
ENST00000524903.2:n.1837C>T
|
|
|
ENST00000528807.2:n.218C>T
|
|
|
ENST00000530040.2:n.479+259C>T
|
|
|
ENST00000533371.6:c.-168C>T
|
ENSP00000437066.1:n.-168C>T
|
|
ENST00000534644.6:n.510C>T
|
|
|
ENST00000642892.1:c.-168C>T
|
ENSP00000494165.1:n.-168C>T
|
|
ENST00000643439.1:c.*302C>T
|
ENSP00000495849.1:n.*302C>T
|
|
ENST00000643479.1:n.591C>T
|
|
|
ENST00000643516.1:c.395+201C>T
|
|
|
ENST00000644151.1:n.2001C>T
|
|
|
ENST00000644218.1:c.562C>T
|
ENSP00000493574.1:p.Pro188Ser
|
|
ENST00000644683.1:c.*15C>T
|
ENSP00000494085.1:n.*15C>T
|
|
ENST00000644810.1:c.283C>T
|
ENSP00000495895.1:p.Pro95Ser
|
|
ENST00000644831.1:n.738C>T
|
|
|
ENST00000644933.1:c.-168C>T
|
ENSP00000496133.1:n.-168C>T
|
|
ENST00000645020.1:n.1737C>T
|
|
|
ENST00000645285.1:c.-168C>T
|
ENSP00000495058.1:n.-168C>T
|
|
ENST00000645331.1:n.928C>T
|
|
|
ENST00000645620.1:c.-168C>T
|
ENSP00000493657.1:n.-168C>T
|
|
ENST00000646777.1:n.738C>T
|
|
|
ENST00000647016.1:n.1042C>T
|
|
|
ENST00000647152.1:c.-168C>T
|
ENSP00000495893.1:n.-168C>T
|
|
ENST00000647209.1:c.*431C>T
|
ENSP00000495558.1:n.*431C>T
|
|
ENST00000647346.1:n.1582C>T
|
|
|
ENST00000299427.10:c.562C>T
|
ENSP00000299427.6:p.Pro188Ser
|
|
ENST00000428886.6:n.731C>T
|
|
|
ENST00000436873.6:c.450+259C>T
|
ENSP00000398136.2:n.450+259C>T
|
|
ENST00000524788.1:n.262C>T
|
|
|
ENST00000528571.5:c.*302C>T
|
ENSP00000434647.1:n.*302C>T
|
|
ENST00000528807.1:n.112C>T
|
|
|
ENST00000533371.5:c.-168C>T
|
ENSP00000437066.1:n.-168C>T
|
|
ENST00000534644.5:n.547C>T
|
|
|
ENST00000611494.4:c.562C>T
|
ENSP00000484546.1:p.Pro188Ser
|
|
NM_000391.3:c.562C>T
|
NP_000382.3:p.Pro188Ser
|
|
NM_000391.4:c.562C>T
MANE Select
|
NP_000382.3:p.Pro188Ser
|
|