ENST00000367698.4:c.1073A>T
MANE Select
|
ENSP00000356671.3:p.Glu358Val
|
|
ENST00000367698.3:c.1073A>T
|
ENSP00000356671.3:p.Glu358Val
|
|
ENST00000617423.4:c.560-2139A>T
|
ENSP00000478688.1:n.560-2139A>T
|
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NM_000488.3:c.1073A>T , LRG_577t1:c.1073A>T
|
NP_000479.1:p.Glu358Val
|
|
XM_005245198.2:c.929A>T
|
XP_005245255.1:p.Glu310Val
|
|
NM_001365052.1:c.929A>T
|
NP_001351981.1:p.Glu310Val
|
|
NM_000488.4:c.1073A>T
MANE Select
|
NP_000479.1:p.Glu358Val
|
|
NM_001365052.2:c.929A>T
|
NP_001351981.1:p.Glu310Val
|
|
NM_001386302.1:c.1196A>T
|
NP_001373231.1:p.Glu399Val
|
|
NM_001386303.1:c.1154A>T
|
NP_001373232.1:p.Glu385Val
|
|
NM_001386304.1:c.1052A>T
|
NP_001373233.1:p.Glu351Val
|
|
NM_001386305.1:c.1016A>T
|
NP_001373234.1:p.Glu339Val
|
|
NM_001386306.1:c.857A>T
|
NP_001373235.1:p.Glu286Val
|
|