ENST00000367698.4:c.1338A>C
MANE Select
|
ENSP00000356671.3:p.Glu446Asp
|
|
ENST00000367698.3:c.1338A>C
|
ENSP00000356671.3:p.Glu446Asp
|
|
ENST00000617423.4:c.723A>C
|
ENSP00000478688.1:p.Glu241Asp
|
|
NM_000488.3:c.1338A>C , LRG_577t1:c.1338A>C
|
NP_000479.1:p.Glu446Asp
|
|
XM_005245198.2:c.1194A>C
|
XP_005245255.1:p.Glu398Asp
|
|
NM_001365052.1:c.1194A>C
|
NP_001351981.1:p.Glu398Asp
|
|
NM_000488.4:c.1338A>C
MANE Select
|
NP_000479.1:p.Glu446Asp
|
|
NM_001365052.2:c.1194A>C
|
NP_001351981.1:p.Glu398Asp
|
|
NM_001386302.1:c.1461A>C
|
NP_001373231.1:p.Glu487Asp
|
|
NM_001386303.1:c.1419A>C
|
NP_001373232.1:p.Glu473Asp
|
|
NM_001386304.1:c.1317A>C
|
NP_001373233.1:p.Glu439Asp
|
|
NM_001386305.1:c.1281A>C
|
NP_001373234.1:p.Glu427Asp
|
|
NM_001386306.1:c.1122A>C
|
NP_001373235.1:p.Glu374Asp
|
|