ENST00000682565.1:c.10077T>A
|
ENSP00000507671.1:p.His3359Gln
|
|
ENST00000682801.1:c.10077T>A
|
ENSP00000507862.1:p.His3359Gln
|
|
ENST00000682859.1:c.10077T>A
|
ENSP00000508222.1:p.His3359Gln
|
|
ENST00000683791.1:c.3163T>A
|
|
|
ENST00000684460.1:c.7358T>A
|
|
|
ENST00000684548.1:c.10077T>A
|
ENSP00000507421.1:p.His3359Gln
|
|
ENST00000684590.1:c.4524T>A
|
ENSP00000507376.1:p.His1508Gln
|
|
ENST00000684656.1:c.7403T>A
|
|
|
ENST00000613296.6:c.10458T>A
MANE Select
|
ENSP00000482968.1:p.His3486Gln
|
|
ENST00000651057.1:c.612T>A
|
ENSP00000498504.1:p.His204Gln
|
|
ENST00000651434.1:c.1814T>A
|
|
|
ENST00000652487.1:c.1555T>A
|
|
|
ENST00000423048.5:c.3949T>A
|
ENSP00000399833.1:n.3949T>A
|
|
ENST00000484298.5:c.10332T>A
|
ENSP00000478155.1:p.His3444Gln
|
|
ENST00000613296.4:c.10458T>A
|
ENSP00000482968.1:p.His3486Gln
|
|
ENST00000614410.4:c.10458T>A
|
ENSP00000479094.1:p.His3486Gln
|
|
ENST00000620466.4:n.4261T>A
|
|
|
NM_015120.4:c.10461T>A , LRG_741t1:c.10461T>A
|
NP_055935.4:p.His3487Gln
|
|
NM_001378454.1:c.10458T>A
MANE Select
|
NP_001365383.1:p.His3486Gln
|
|