ENST00000682565.1:c.7641A>G
|
ENSP00000507671.1:p.Glu2547=
|
|
ENST00000682801.1:c.7641A>G
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ENSP00000507862.1:p.Glu2547=
|
|
ENST00000682859.1:c.7641A>G
|
ENSP00000508222.1:p.Glu2547=
|
|
ENST00000683791.1:c.1033A>G
|
|
|
ENST00000684460.1:c.5093A>G
|
|
|
ENST00000684548.1:c.7641A>G
|
ENSP00000507421.1:p.Glu2547=
|
|
ENST00000684590.1:c.2088A>G
|
ENSP00000507376.1:p.Glu696=
|
|
ENST00000684656.1:c.5093A>G
|
|
|
ENST00000613296.6:c.8022A>G
MANE Select
|
ENSP00000482968.1:p.Glu2674=
|
|
ENST00000651434.1:c.896-29794A>G
|
|
|
ENST00000423048.5:c.2853A>G
|
ENSP00000399833.1:p.Glu951=
|
|
ENST00000484298.5:c.7896A>G
|
ENSP00000478155.1:p.Glu2632=
|
|
ENST00000613296.4:c.8022A>G
|
ENSP00000482968.1:p.Glu2674=
|
|
ENST00000614410.4:c.8022A>G
|
ENSP00000479094.1:p.Glu2674=
|
|
ENST00000620466.4:n.1825A>G
|
|
|
NM_015120.4:c.8025A>G , LRG_741t1:c.8025A>G
|
NP_055935.4:p.Glu2675=
|
|
NM_001378454.1:c.8022A>G
MANE Select
|
NP_001365383.1:p.Glu2674=
|
|