ENST00000682565.1:c.7332A>C
|
ENSP00000507671.1:p.Glu2444Asp
|
|
ENST00000682801.1:c.7332A>C
|
ENSP00000507862.1:p.Glu2444Asp
|
|
ENST00000682859.1:c.7332A>C
|
ENSP00000508222.1:p.Glu2444Asp
|
|
ENST00000683791.1:c.724A>C
|
|
|
ENST00000684460.1:c.4784A>C
|
|
|
ENST00000684548.1:c.7332A>C
|
ENSP00000507421.1:p.Glu2444Asp
|
|
ENST00000684590.1:c.1779A>C
|
ENSP00000507376.1:p.Glu593Asp
|
|
ENST00000684656.1:c.4784A>C
|
|
|
ENST00000613296.6:c.7713A>C
MANE Select
|
ENSP00000482968.1:p.Glu2571Asp
|
|
ENST00000651434.1:c.896-30103A>C
|
|
|
ENST00000423048.5:c.2544A>C
|
ENSP00000399833.1:p.Glu848Asp
|
|
ENST00000484298.5:c.7587A>C
|
ENSP00000478155.1:p.Glu2529Asp
|
|
ENST00000613296.4:c.7713A>C
|
ENSP00000482968.1:p.Glu2571Asp
|
|
ENST00000614410.4:c.7713A>C
|
ENSP00000479094.1:p.Glu2571Asp
|
|
ENST00000620466.4:n.1516A>C
|
|
|
NM_015120.4:c.7716A>C , LRG_741t1:c.7716A>C
|
NP_055935.4:p.Glu2572Asp
|
|
NM_001378454.1:c.7713A>C
MANE Select
|
NP_001365383.1:p.Glu2571Asp
|
|