|
ENST00000367698.4:c.859G=
MANE Select
|
ENSP00000356671.3:p.Glu287=
|
|
|
ENST00000367698.3:c.859G=
|
ENSP00000356671.3:p.Glu287=
|
|
|
ENST00000487183.1:n.510G=
|
|
|
|
ENST00000617423.4:c.559+2018G=
|
ENSP00000478688.1:n.559+2018G=
|
|
|
NM_000488.3:c.859G= , LRG_577t1:c.859G=
|
NP_000479.1:p.Glu287=
|
|
|
XM_005245198.2:c.715G=
|
XP_005245255.1:p.Glu239=
|
|
|
NM_001365052.1:c.715G=
|
NP_001351981.1:p.Glu239=
|
|
|
NM_000488.4:c.859G=
MANE Select
|
NP_000479.1:p.Glu287=
|
|
|
NM_001365052.2:c.715G=
|
NP_001351981.1:p.Glu239=
|
|
|
NM_001386302.1:c.982G=
|
NP_001373231.1:p.Glu328=
|
|
|
NM_001386303.1:c.940G=
|
NP_001373232.1:p.Glu314=
|
|
|
NM_001386304.1:c.838G=
|
NP_001373233.1:p.Glu280=
|
|
|
NM_001386305.1:c.802G=
|
NP_001373234.1:p.Glu268=
|
|
|
NM_001386306.1:c.643G=
|
NP_001373235.1:p.Glu215=
|
|
