|
ENST00000682424.1:c.418C>A
|
ENSP00000507321.1:p.Pro140Thr
|
|
|
ENST00000299427.12:c.532C>A
MANE Select
|
ENSP00000299427.6:p.Pro178Thr
|
|
|
ENST00000428886.7:n.767C>A
|
|
|
|
ENST00000436873.7:c.312+171C>A
|
|
|
|
ENST00000524788.2:n.1691C>A
|
|
|
|
ENST00000524903.2:n.1807C>A
|
|
|
|
ENST00000528807.2:n.188C>A
|
|
|
|
ENST00000530040.2:n.479+229C>A
|
|
|
|
ENST00000533371.6:c.-198C>A
|
ENSP00000437066.1:n.-198C>A
|
|
|
ENST00000534644.6:n.480C>A
|
|
|
|
ENST00000642892.1:c.-198C>A
|
ENSP00000494165.1:n.-198C>A
|
|
|
ENST00000643439.1:c.*272C>A
|
ENSP00000495849.1:n.*272C>A
|
|
|
ENST00000643479.1:n.561C>A
|
|
|
|
ENST00000643516.1:c.395+171C>A
|
|
|
|
ENST00000644151.1:n.1971C>A
|
|
|
|
ENST00000644218.1:c.532C>A
|
ENSP00000493574.1:p.Pro178Thr
|
|
|
ENST00000644683.1:c.474C>A
|
ENSP00000494085.1:p.Pro158=
|
|
|
ENST00000644810.1:c.253C>A
|
ENSP00000495895.1:p.Pro85Thr
|
|
|
ENST00000644831.1:n.708C>A
|
|
|
|
ENST00000644933.1:c.-198C>A
|
ENSP00000496133.1:n.-198C>A
|
|
|
ENST00000645020.1:n.1707C>A
|
|
|
|
ENST00000645285.1:c.-198C>A
|
ENSP00000495058.1:n.-198C>A
|
|
|
ENST00000645331.1:n.898C>A
|
|
|
|
ENST00000645620.1:c.-198C>A
|
ENSP00000493657.1:n.-198C>A
|
|
|
ENST00000646777.1:n.708C>A
|
|
|
|
ENST00000647016.1:n.1012C>A
|
|
|
|
ENST00000647152.1:c.-198C>A
|
ENSP00000495893.1:n.-198C>A
|
|
|
ENST00000647209.1:c.*401C>A
|
ENSP00000495558.1:n.*401C>A
|
|
|
ENST00000647346.1:n.1552C>A
|
|
|
|
ENST00000299427.10:c.532C>A
|
ENSP00000299427.6:p.Pro178Thr
|
|
|
ENST00000428886.6:n.701C>A
|
|
|
|
ENST00000436873.6:c.450+229C>A
|
ENSP00000398136.2:n.450+229C>A
|
|
|
ENST00000524788.1:n.232C>A
|
|
|
|
ENST00000528571.5:c.*272C>A
|
ENSP00000434647.1:n.*272C>A
|
|
|
ENST00000528807.1:n.82C>A
|
|
|
|
ENST00000533371.5:c.-198C>A
|
ENSP00000437066.1:n.-198C>A
|
|
|
ENST00000534644.5:n.517C>A
|
|
|
|
ENST00000611494.4:c.532C>A
|
ENSP00000484546.1:p.Pro178Thr
|
|
|
NM_000391.3:c.532C>A
|
NP_000382.3:p.Pro178Thr
|
|
|
NM_000391.4:c.532C>A
MANE Select
|
NP_000382.3:p.Pro178Thr
|
|
