|
ENST00000367698.4:c.1024G=
MANE Select
|
ENSP00000356671.3:p.Glu342=
|
|
|
ENST00000367698.3:c.1024G=
|
ENSP00000356671.3:p.Glu342=
|
|
|
ENST00000617423.4:c.559+2183G=
|
ENSP00000478688.1:n.559+2183G=
|
|
|
NM_000488.3:c.1024G= , LRG_577t1:c.1024G=
|
NP_000479.1:p.Glu342=
|
|
|
XM_005245198.2:c.880G=
|
XP_005245255.1:p.Glu294=
|
|
|
NM_001365052.1:c.880G=
|
NP_001351981.1:p.Glu294=
|
|
|
NM_000488.4:c.1024G=
MANE Select
|
NP_000479.1:p.Glu342=
|
|
|
NM_001365052.2:c.880G=
|
NP_001351981.1:p.Glu294=
|
|
|
NM_001386302.1:c.1147G=
|
NP_001373231.1:p.Glu383=
|
|
|
NM_001386303.1:c.1105G=
|
NP_001373232.1:p.Glu369=
|
|
|
NM_001386304.1:c.1003G=
|
NP_001373233.1:p.Glu335=
|
|
|
NM_001386305.1:c.967G=
|
NP_001373234.1:p.Glu323=
|
|
|
NM_001386306.1:c.808G=
|
NP_001373235.1:p.Glu270=
|
|
