|
ENST00000367698.4:c.982G=
MANE Select
|
ENSP00000356671.3:p.Glu328=
|
|
|
ENST00000367698.3:c.982G=
|
ENSP00000356671.3:p.Glu328=
|
|
|
ENST00000617423.4:c.559+2141G=
|
ENSP00000478688.1:n.559+2141G=
|
|
|
NM_000488.3:c.982G= , LRG_577t1:c.982G=
|
NP_000479.1:p.Glu328=
|
|
|
XM_005245198.2:c.838G=
|
XP_005245255.1:p.Glu280=
|
|
|
NM_001365052.1:c.838G=
|
NP_001351981.1:p.Glu280=
|
|
|
NM_000488.4:c.982G=
MANE Select
|
NP_000479.1:p.Glu328=
|
|
|
NM_001365052.2:c.838G=
|
NP_001351981.1:p.Glu280=
|
|
|
NM_001386302.1:c.1105G=
|
NP_001373231.1:p.Glu369=
|
|
|
NM_001386303.1:c.1063G=
|
NP_001373232.1:p.Glu355=
|
|
|
NM_001386304.1:c.961G=
|
NP_001373233.1:p.Glu321=
|
|
|
NM_001386305.1:c.925G=
|
NP_001373234.1:p.Glu309=
|
|
|
NM_001386306.1:c.766G=
|
NP_001373235.1:p.Glu256=
|
|
