ENST00000682565.1:c.10193A>T
|
ENSP00000507671.1:p.His3398Leu
|
|
ENST00000682801.1:c.10193A>T
|
ENSP00000507862.1:p.His3398Leu
|
|
ENST00000682859.1:c.10193A>T
|
ENSP00000508222.1:p.His3398Leu
|
|
ENST00000683791.1:c.3279A>T
|
|
|
ENST00000684460.1:c.7474A>T
|
|
|
ENST00000684548.1:c.10193A>T
|
ENSP00000507421.1:p.His3398Leu
|
|
ENST00000684590.1:c.4640A>T
|
ENSP00000507376.1:p.His1547Leu
|
|
ENST00000684656.1:c.7519A>T
|
|
|
ENST00000613296.6:c.10574A>T
MANE Select
|
ENSP00000482968.1:p.His3525Leu
|
|
ENST00000651057.1:c.728A>T
|
ENSP00000498504.1:p.His243Leu
|
|
ENST00000651434.1:c.1930A>T
|
|
|
ENST00000652487.1:c.1671A>T
|
|
|
ENST00000423048.5:c.4065A>T
|
ENSP00000399833.1:n.4065A>T
|
|
ENST00000484298.5:c.10448A>T
|
ENSP00000478155.1:p.His3483Leu
|
|
ENST00000613296.4:c.10574A>T
|
ENSP00000482968.1:p.His3525Leu
|
|
ENST00000614410.4:c.10574A>T
|
ENSP00000479094.1:p.His3525Leu
|
|
ENST00000620466.4:n.4377A>T
|
|
|
NM_015120.4:c.10577A>T , LRG_741t1:c.10577A>T
|
NP_055935.4:p.His3526Leu
|
|
NM_001378454.1:c.10574A>T
MANE Select
|
NP_001365383.1:p.His3525Leu
|
|