ENST00000682565.1:c.11703A>G
|
ENSP00000507671.1:p.Leu3901=
|
|
ENST00000682801.1:c.11167-779A>G
|
ENSP00000507862.1:n.11167-779A>G
|
|
ENST00000682859.1:c.11703A>G
|
ENSP00000508222.1:p.Leu3901=
|
|
ENST00000683791.1:c.4789A>G
|
|
|
ENST00000684460.1:c.8984A>G
|
|
|
ENST00000684548.1:c.11703A>G
|
ENSP00000507421.1:p.Leu3901=
|
|
ENST00000684590.1:c.6150A>G
|
ENSP00000507376.1:p.Leu2050=
|
|
ENST00000684656.1:c.9168A>G
|
|
|
ENST00000613296.6:c.12084A>G
MANE Select
|
ENSP00000482968.1:p.Leu4028=
|
|
ENST00000651057.1:c.2238A>G
|
ENSP00000498504.1:p.Leu746=
|
|
ENST00000651434.1:c.3440A>G
|
|
|
ENST00000651750.1:c.1260+525A>G
|
|
|
ENST00000652487.1:c.3255A>G
|
|
|
ENST00000464408.3:n.259A>G
|
|
|
ENST00000484298.5:c.11958A>G
|
ENSP00000478155.1:p.Leu3986=
|
|
ENST00000613296.4:c.12084A>G
|
ENSP00000482968.1:p.Leu4028=
|
|
ENST00000620466.4:n.5887A>G
|
|
|
NM_015120.4:c.12087A>G , LRG_741t1:c.12087A>G
|
NP_055935.4:p.Leu4029=
|
|
NM_001378454.1:c.12084A>G
MANE Select
|
NP_001365383.1:p.Leu4028=
|
|