ENST00000682565.1:c.11701C>T
|
ENSP00000507671.1:p.Leu3901=
|
|
ENST00000682801.1:c.11167-781C>T
|
ENSP00000507862.1:n.11167-781C>T
|
|
ENST00000682859.1:c.11701C>T
|
ENSP00000508222.1:p.Leu3901=
|
|
ENST00000683791.1:c.4787C>T
|
|
|
ENST00000684460.1:c.8982C>T
|
|
|
ENST00000684548.1:c.11701C>T
|
ENSP00000507421.1:p.Leu3901=
|
|
ENST00000684590.1:c.6148C>T
|
ENSP00000507376.1:p.Leu2050=
|
|
ENST00000684656.1:c.9166C>T
|
|
|
ENST00000613296.6:c.12082C>T
MANE Select
|
ENSP00000482968.1:p.Leu4028=
|
|
ENST00000651057.1:c.2236C>T
|
ENSP00000498504.1:p.Leu746=
|
|
ENST00000651434.1:c.3438C>T
|
|
|
ENST00000651750.1:c.1260+523C>T
|
|
|
ENST00000652487.1:c.3253C>T
|
|
|
ENST00000464408.3:n.257C>T
|
|
|
ENST00000484298.5:c.11956C>T
|
ENSP00000478155.1:p.Leu3986=
|
|
ENST00000613296.4:c.12082C>T
|
ENSP00000482968.1:p.Leu4028=
|
|
ENST00000620466.4:n.5885C>T
|
|
|
NM_015120.4:c.12085C>T , LRG_741t1:c.12085C>T
|
NP_055935.4:p.Leu4029=
|
|
NM_001378454.1:c.12082C>T
MANE Select
|
NP_001365383.1:p.Leu4028=
|
|