ENST00000367698.4:c.1023T>G
MANE Select
|
ENSP00000356671.3:p.Asp341Glu
|
|
ENST00000367698.3:c.1023T>G
|
ENSP00000356671.3:p.Asp341Glu
|
|
ENST00000617423.4:c.559+2182T>G
|
ENSP00000478688.1:n.559+2182T>G
|
|
NM_000488.3:c.1023T>G , LRG_577t1:c.1023T>G
|
NP_000479.1:p.Asp341Glu
|
|
XM_005245198.2:c.879T>G
|
XP_005245255.1:p.Asp293Glu
|
|
NM_001365052.1:c.879T>G
|
NP_001351981.1:p.Asp293Glu
|
|
NM_000488.4:c.1023T>G
MANE Select
|
NP_000479.1:p.Asp341Glu
|
|
NM_001365052.2:c.879T>G
|
NP_001351981.1:p.Asp293Glu
|
|
NM_001386302.1:c.1146T>G
|
NP_001373231.1:p.Asp382Glu
|
|
NM_001386303.1:c.1104T>G
|
NP_001373232.1:p.Asp368Glu
|
|
NM_001386304.1:c.1002T>G
|
NP_001373233.1:p.Asp334Glu
|
|
NM_001386305.1:c.966T>G
|
NP_001373234.1:p.Asp322Glu
|
|
NM_001386306.1:c.807T>G
|
NP_001373235.1:p.Asp269Glu
|
|