ENST00000682565.1:c.11729T>A
|
ENSP00000507671.1:p.Leu3910His
|
|
ENST00000682801.1:c.11167-753T>A
|
ENSP00000507862.1:n.11167-753T>A
|
|
ENST00000682859.1:c.11729T>A
|
ENSP00000508222.1:p.Leu3910His
|
|
ENST00000683791.1:c.4815T>A
|
|
|
ENST00000684460.1:c.9010T>A
|
|
|
ENST00000684548.1:c.11729T>A
|
ENSP00000507421.1:p.Leu3910His
|
|
ENST00000684590.1:c.6176T>A
|
ENSP00000507376.1:p.Leu2059His
|
|
ENST00000684656.1:c.9194T>A
|
|
|
ENST00000613296.6:c.12110T>A
MANE Select
|
ENSP00000482968.1:p.Leu4037His
|
|
ENST00000651057.1:c.2264T>A
|
ENSP00000498504.1:p.Leu755His
|
|
ENST00000651434.1:c.3466T>A
|
|
|
ENST00000651750.1:c.1260+551T>A
|
|
|
ENST00000652487.1:c.3281T>A
|
|
|
ENST00000464408.3:n.285T>A
|
|
|
ENST00000484298.5:c.11984T>A
|
ENSP00000478155.1:p.Leu3995His
|
|
ENST00000613296.4:c.12110T>A
|
ENSP00000482968.1:p.Leu4037His
|
|
ENST00000620466.4:n.5913T>A
|
|
|
NM_015120.4:c.12113T>A , LRG_741t1:c.12113T>A
|
NP_055935.4:p.Leu4038His
|
|
NM_001378454.1:c.12110T>A
MANE Select
|
NP_001365383.1:p.Leu4037His
|
|