ENST00000367698.4:c.1137A>T
MANE Select
|
ENSP00000356671.3:p.Glu379Asp
|
|
ENST00000367698.3:c.1137A>T
|
ENSP00000356671.3:p.Glu379Asp
|
|
ENST00000617423.4:c.560-2075A>T
|
ENSP00000478688.1:n.560-2075A>T
|
|
NM_000488.3:c.1137A>T , LRG_577t1:c.1137A>T
|
NP_000479.1:p.Glu379Asp
|
|
XM_005245198.2:c.993A>T
|
XP_005245255.1:p.Glu331Asp
|
|
NM_001365052.1:c.993A>T
|
NP_001351981.1:p.Glu331Asp
|
|
NM_000488.4:c.1137A>T
MANE Select
|
NP_000479.1:p.Glu379Asp
|
|
NM_001365052.2:c.993A>T
|
NP_001351981.1:p.Glu331Asp
|
|
NM_001386302.1:c.1260A>T
|
NP_001373231.1:p.Glu420Asp
|
|
NM_001386303.1:c.1218A>T
|
NP_001373232.1:p.Glu406Asp
|
|
NM_001386304.1:c.1116A>T
|
NP_001373233.1:p.Glu372Asp
|
|
NM_001386305.1:c.1080A>T
|
NP_001373234.1:p.Glu360Asp
|
|
NM_001386306.1:c.921A>T
|
NP_001373235.1:p.Glu307Asp
|
|