|
ENST00000367698.4:c.1227A>T
MANE Select
|
ENSP00000356671.3:p.Glu409Asp
|
|
|
ENST00000367698.3:c.1227A>T
|
ENSP00000356671.3:p.Glu409Asp
|
|
|
ENST00000617423.4:c.612A>T
|
ENSP00000478688.1:p.Glu204Asp
|
|
|
NM_000488.3:c.1227A>T , LRG_577t1:c.1227A>T
|
NP_000479.1:p.Glu409Asp
|
|
|
XM_005245198.2:c.1083A>T
|
XP_005245255.1:p.Glu361Asp
|
|
|
NM_001365052.1:c.1083A>T
|
NP_001351981.1:p.Glu361Asp
|
|
|
NM_000488.4:c.1227A>T
MANE Select
|
NP_000479.1:p.Glu409Asp
|
|
|
NM_001365052.2:c.1083A>T
|
NP_001351981.1:p.Glu361Asp
|
|
|
NM_001386302.1:c.1350A>T
|
NP_001373231.1:p.Glu450Asp
|
|
|
NM_001386303.1:c.1308A>T
|
NP_001373232.1:p.Glu436Asp
|
|
|
NM_001386304.1:c.1206A>T
|
NP_001373233.1:p.Glu402Asp
|
|
|
NM_001386305.1:c.1170A>T
|
NP_001373234.1:p.Glu390Asp
|
|
|
NM_001386306.1:c.1011A>T
|
NP_001373235.1:p.Glu337Asp
|
|
