ENST00000367698.4:c.1094A=
MANE Select
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ENSP00000356671.3:p.Glu365=
|
|
ENST00000367698.3:c.1094A=
|
ENSP00000356671.3:p.Glu365=
|
|
ENST00000617423.4:c.560-2118A=
|
ENSP00000478688.1:n.560-2118A=
|
|
NM_000488.3:c.1094A= , LRG_577t1:c.1094A=
|
NP_000479.1:p.Glu365=
|
|
XM_005245198.2:c.950A=
|
XP_005245255.1:p.Glu317=
|
|
NM_001365052.1:c.950A=
|
NP_001351981.1:p.Glu317=
|
|
NM_000488.4:c.1094A=
MANE Select
|
NP_000479.1:p.Glu365=
|
|
NM_001365052.2:c.950A=
|
NP_001351981.1:p.Glu317=
|
|
NM_001386302.1:c.1217A=
|
NP_001373231.1:p.Glu406=
|
|
NM_001386303.1:c.1175A=
|
NP_001373232.1:p.Glu392=
|
|
NM_001386304.1:c.1073A=
|
NP_001373233.1:p.Glu358=
|
|
NM_001386305.1:c.1037A=
|
NP_001373234.1:p.Glu346=
|
|
NM_001386306.1:c.878A=
|
NP_001373235.1:p.Glu293=
|
|