|
ENST00000367698.4:c.1239A=
MANE Select
|
ENSP00000356671.3:p.Glu413=
|
|
|
ENST00000367698.3:c.1239A=
|
ENSP00000356671.3:p.Glu413=
|
|
|
ENST00000617423.4:c.624A=
|
ENSP00000478688.1:p.Glu208=
|
|
|
NM_000488.3:c.1239A= , LRG_577t1:c.1239A=
|
NP_000479.1:p.Glu413=
|
|
|
XM_005245198.2:c.1095A=
|
XP_005245255.1:p.Glu365=
|
|
|
NM_001365052.1:c.1095A=
|
NP_001351981.1:p.Glu365=
|
|
|
NM_000488.4:c.1239A=
MANE Select
|
NP_000479.1:p.Glu413=
|
|
|
NM_001365052.2:c.1095A=
|
NP_001351981.1:p.Glu365=
|
|
|
NM_001386302.1:c.1362A=
|
NP_001373231.1:p.Glu454=
|
|
|
NM_001386303.1:c.1320A=
|
NP_001373232.1:p.Glu440=
|
|
|
NM_001386304.1:c.1218A=
|
NP_001373233.1:p.Glu406=
|
|
|
NM_001386305.1:c.1182A=
|
NP_001373234.1:p.Glu394=
|
|
|
NM_001386306.1:c.1023A=
|
NP_001373235.1:p.Glu341=
|
|
