ENST00000463956.2:n.543G>T
|
|
|
ENST00000484513.2:n.2234G>T
|
|
|
ENST00000699084.1:n.1845G>T
|
|
|
ENST00000699085.1:n.1621G>T
|
|
|
ENST00000699086.1:c.537G>T
|
|
|
ENST00000396334.8:c.756G>T
|
ENSP00000379625.4:p.Leu252=
|
|
ENST00000416282.3:n.859G>T
|
|
|
ENST00000417037.8:c.621G>T
|
ENSP00000401399.4:p.Leu207=
|
|
ENST00000421516.3:c.780G>T
|
ENSP00000391753.3:p.Leu260=
|
|
ENST00000650112.2:c.440G>T
|
ENSP00000497991.2:p.Ter147Leu
|
|
ENST00000650905.2:c.756G>T
MANE Select
|
ENSP00000498360.2:p.Leu252=
|
|
ENST00000651800.2:c.575G>T
|
ENSP00000499012.2:p.Ter192Leu
|
|
ENST00000652213.1:c.737G>T
|
ENSP00000498576.1:p.Ter246Leu
|
|
ENST00000652590.1:n.984G>T
|
|
|
ENST00000396334.7:c.795G>T
|
ENSP00000379625.3:p.Leu265=
|
|
ENST00000416282.2:n.859G>T
|
|
|
ENST00000417037.6:c.819G>T
|
ENSP00000401399.2:p.Leu273=
|
|
ENST00000421516.1:c.816G>T
|
ENSP00000391753.1:p.Leu272=
|
|
ENST00000424893.5:c.660G>T
|
ENSP00000389979.1:p.Leu220=
|
|
ENST00000443433.6:c.614G>T
|
ENSP00000390565.2:p.Ter205Leu
|
|
ENST00000463956.1:n.469G>T
|
|
|
ENST00000481122.5:n.549G>T
|
|
|
ENST00000484513.1:n.1446G>T
|
|
|
ENST00000495303.5:c.479G>T
|
ENSP00000417848.1:p.Ter160Leu
|
|
NM_001172566.1:c.479G>T
|
NP_001166037.1:p.Ter160Leu
|
|
NM_001172567.1:c.819G>T , LRG_157t1:c.819G>T
|
NP_001166038.1:p.Leu273=
|
|
NM_001172568.1:c.660G>T
|
NP_001166039.1:p.Leu220=
|
|
NM_001172569.1:c.614G>T
|
NP_001166040.1:p.Ter205Leu
|
|
NM_002468.4:c.795G>T
|
NP_002459.2:p.Leu265=
|
|
XM_005265172.1:c.776G>T
|
XP_005265229.1:p.Ter259Leu
|
|
XM_006713170.1:c.641G>T
|
XP_006713233.1:p.Ter214Leu
|
|
NM_001172566.2:c.440G>T
|
NP_001166037.2:p.Ter147Leu
|
|
NM_001172567.2:c.780G>T
|
NP_001166038.2:p.Leu260=
|
|
NM_001172568.2:c.621G>T
|
NP_001166039.2:p.Leu207=
|
|
NM_001172569.2:c.575G>T
|
NP_001166040.2:p.Ter192Leu
|
|
NM_001365876.1:c.737G>T
|
NP_001352805.1:p.Ter246Leu
|
|
NM_001365877.1:c.602G>T
|
NP_001352806.1:p.Ter201Leu
|
|
NM_002468.5:c.756G>T
MANE Select
|
NP_002459.3:p.Leu252=
|
|
NM_001172569.3:c.575G>T
|
NP_001166040.2:p.Ter192Leu
|
|
NM_001374787.1:c.713G>T
|
NP_001361716.1:p.Ter238Leu
|
|
NM_001374788.1:c.288G>T
|
NP_001361717.1:p.Leu96=
|
|
NR_164663.1:n.439G>T
|
|
|