ENST00000682565.1:c.10144C>G
|
ENSP00000507671.1:p.His3382Asp
|
|
ENST00000682801.1:c.10144C>G
|
ENSP00000507862.1:p.His3382Asp
|
|
ENST00000682859.1:c.10144C>G
|
ENSP00000508222.1:p.His3382Asp
|
|
ENST00000683791.1:c.3230C>G
|
|
|
ENST00000684460.1:c.7425C>G
|
|
|
ENST00000684548.1:c.10144C>G
|
ENSP00000507421.1:p.His3382Asp
|
|
ENST00000684590.1:c.4591C>G
|
ENSP00000507376.1:p.His1531Asp
|
|
ENST00000684656.1:c.7470C>G
|
|
|
ENST00000613296.6:c.10525C>G
MANE Select
|
ENSP00000482968.1:p.His3509Asp
|
|
ENST00000651057.1:c.679C>G
|
ENSP00000498504.1:p.His227Asp
|
|
ENST00000651434.1:c.1881C>G
|
|
|
ENST00000652487.1:c.1622C>G
|
|
|
ENST00000423048.5:c.4016C>G
|
ENSP00000399833.1:n.4016C>G
|
|
ENST00000484298.5:c.10399C>G
|
ENSP00000478155.1:p.His3467Asp
|
|
ENST00000613296.4:c.10525C>G
|
ENSP00000482968.1:p.His3509Asp
|
|
ENST00000614410.4:c.10525C>G
|
ENSP00000479094.1:p.His3509Asp
|
|
ENST00000620466.4:n.4328C>G
|
|
|
NM_015120.4:c.10528C>G , LRG_741t1:c.10528C>G
|
NP_055935.4:p.His3510Asp
|
|
NM_001378454.1:c.10525C>G
MANE Select
|
NP_001365383.1:p.His3509Asp
|
|