|
ENST00000367698.4:c.891A>T
MANE Select
|
ENSP00000356671.3:p.Glu297Asp
|
|
|
ENST00000367698.3:c.891A>T
|
ENSP00000356671.3:p.Glu297Asp
|
|
|
ENST00000487183.1:n.542A>T
|
|
|
|
ENST00000617423.4:c.559+2050A>T
|
ENSP00000478688.1:n.559+2050A>T
|
|
|
NM_000488.3:c.891A>T , LRG_577t1:c.891A>T
|
NP_000479.1:p.Glu297Asp
|
|
|
XM_005245198.2:c.747A>T
|
XP_005245255.1:p.Glu249Asp
|
|
|
NM_001365052.1:c.747A>T
|
NP_001351981.1:p.Glu249Asp
|
|
|
NM_000488.4:c.891A>T
MANE Select
|
NP_000479.1:p.Glu297Asp
|
|
|
NM_001365052.2:c.747A>T
|
NP_001351981.1:p.Glu249Asp
|
|
|
NM_001386302.1:c.1014A>T
|
NP_001373231.1:p.Glu338Asp
|
|
|
NM_001386303.1:c.972A>T
|
NP_001373232.1:p.Glu324Asp
|
|
|
NM_001386304.1:c.870A>T
|
NP_001373233.1:p.Glu290Asp
|
|
|
NM_001386305.1:c.834A>T
|
NP_001373234.1:p.Glu278Asp
|
|
|
NM_001386306.1:c.675A>T
|
NP_001373235.1:p.Glu225Asp
|
|
