|
ENST00000682424.1:c.772+7C>T
|
ENSP00000507321.1:n.772+7C>T
|
|
|
ENST00000299427.12:c.886+7C>T
MANE Select
|
ENSP00000299427.6:n.886+7C>T
|
|
|
ENST00000436873.7:c.313-580C>T
|
|
|
|
ENST00000524788.2:n.2052C>T
|
|
|
|
ENST00000524903.2:n.2168C>T
|
|
|
|
ENST00000528807.2:n.549C>T
|
|
|
|
ENST00000530040.2:n.480-151C>T
|
|
|
|
ENST00000533371.6:c.157+7C>T
|
ENSP00000437066.1:n.157+7C>T
|
|
|
ENST00000642892.1:c.157+7C>T
|
ENSP00000494165.1:n.157+7C>T
|
|
|
ENST00000643439.1:c.*626+7C>T
|
ENSP00000495849.1:n.*626+7C>T
|
|
|
ENST00000643479.1:n.922C>T
|
|
|
|
ENST00000643516.1:c.396-151C>T
|
|
|
|
ENST00000644151.1:n.2332C>T
|
|
|
|
ENST00000644218.1:c.886+7C>T
|
ENSP00000493574.1:n.886+7C>T
|
|
|
ENST00000644683.1:c.*339+7C>T
|
ENSP00000494085.1:n.*339+7C>T
|
|
|
ENST00000644810.1:c.607+7C>T
|
ENSP00000495895.1:n.607+7C>T
|
|
|
ENST00000644831.1:n.1062+7C>T
|
|
|
|
ENST00000644933.1:c.157+7C>T
|
ENSP00000496133.1:n.157+7C>T
|
|
|
ENST00000645020.1:n.2183C>T
|
|
|
|
ENST00000645285.1:c.157+7C>T
|
ENSP00000495058.1:n.157+7C>T
|
|
|
ENST00000645331.1:n.1259C>T
|
|
|
|
ENST00000645620.1:c.157+7C>T
|
ENSP00000493657.1:n.157+7C>T
|
|
|
ENST00000646777.1:n.1069C>T
|
|
|
|
ENST00000647016.1:n.1366+7C>T
|
|
|
|
ENST00000647152.1:c.157+7C>T
|
ENSP00000495893.1:n.157+7C>T
|
|
|
ENST00000647209.1:c.*755+7C>T
|
ENSP00000495558.1:n.*755+7C>T
|
|
|
ENST00000647346.1:n.1906+7C>T
|
|
|
|
ENST00000299427.10:c.886+7C>T
|
ENSP00000299427.6:n.886+7C>T
|
|
|
ENST00000436873.6:c.451-151C>T
|
ENSP00000398136.2:n.451-151C>T
|
|
|
ENST00000528807.1:n.443C>T
|
|
|
|
ENST00000533371.5:c.157+7C>T
|
ENSP00000437066.1:n.157+7C>T
|
|
|
ENST00000611494.4:c.886+7C>T
|
ENSP00000484546.1:n.886+7C>T
|
|
|
NM_000391.3:c.886+7C>T
|
NP_000382.3:n.886+7C>T
|
|
|
NM_000391.4:c.886+7C>T
MANE Select
|
NP_000382.3:n.886+7C>T
|
|
