ENST00000682565.1:c.11733G>T
|
ENSP00000507671.1:p.Gln3911His
|
|
ENST00000682801.1:c.11167-749G>T
|
ENSP00000507862.1:n.11167-749G>T
|
|
ENST00000682859.1:c.11733G>T
|
ENSP00000508222.1:p.Gln3911His
|
|
ENST00000683791.1:c.4819G>T
|
|
|
ENST00000684460.1:c.9014G>T
|
|
|
ENST00000684548.1:c.11733G>T
|
ENSP00000507421.1:p.Gln3911His
|
|
ENST00000684590.1:c.6180G>T
|
ENSP00000507376.1:p.Gln2060His
|
|
ENST00000684656.1:c.9198G>T
|
|
|
ENST00000613296.6:c.12114G>T
MANE Select
|
ENSP00000482968.1:p.Gln4038His
|
|
ENST00000651057.1:c.2268G>T
|
ENSP00000498504.1:p.Gln756His
|
|
ENST00000651434.1:c.3470G>T
|
|
|
ENST00000651750.1:c.1260+555G>T
|
|
|
ENST00000652487.1:c.3285G>T
|
|
|
ENST00000464408.3:n.289G>T
|
|
|
ENST00000484298.5:c.11988G>T
|
ENSP00000478155.1:p.Gln3996His
|
|
ENST00000613296.4:c.12114G>T
|
ENSP00000482968.1:p.Gln4038His
|
|
ENST00000620466.4:n.5917G>T
|
|
|
NM_015120.4:c.12117G>T , LRG_741t1:c.12117G>T
|
NP_055935.4:p.Gln4039His
|
|
NM_001378454.1:c.12114G>T
MANE Select
|
NP_001365383.1:p.Gln4038His
|
|