ENST00000682565.1:c.11706G>C
|
ENSP00000507671.1:p.Leu3902=
|
|
ENST00000682801.1:c.11167-776G>C
|
ENSP00000507862.1:n.11167-776G>C
|
|
ENST00000682859.1:c.11706G>C
|
ENSP00000508222.1:p.Leu3902=
|
|
ENST00000683791.1:c.4792G>C
|
|
|
ENST00000684460.1:c.8987G>C
|
|
|
ENST00000684548.1:c.11706G>C
|
ENSP00000507421.1:p.Leu3902=
|
|
ENST00000684590.1:c.6153G>C
|
ENSP00000507376.1:p.Leu2051=
|
|
ENST00000684656.1:c.9171G>C
|
|
|
ENST00000613296.6:c.12087G>C
MANE Select
|
ENSP00000482968.1:p.Leu4029=
|
|
ENST00000651057.1:c.2241G>C
|
ENSP00000498504.1:p.Leu747=
|
|
ENST00000651434.1:c.3443G>C
|
|
|
ENST00000651750.1:c.1260+528G>C
|
|
|
ENST00000652487.1:c.3258G>C
|
|
|
ENST00000464408.3:n.262G>C
|
|
|
ENST00000484298.5:c.11961G>C
|
ENSP00000478155.1:p.Leu3987=
|
|
ENST00000613296.4:c.12087G>C
|
ENSP00000482968.1:p.Leu4029=
|
|
ENST00000620466.4:n.5890G>C
|
|
|
NM_015120.4:c.12090G>C , LRG_741t1:c.12090G>C
|
NP_055935.4:p.Leu4030=
|
|
NM_001378454.1:c.12087G>C
MANE Select
|
NP_001365383.1:p.Leu4029=
|
|