ENST00000367698.4:c.1060C=
MANE Select
|
ENSP00000356671.3:p.Arg354=
|
|
ENST00000367698.3:c.1060C=
|
ENSP00000356671.3:p.Arg354=
|
|
ENST00000617423.4:c.560-2152C=
|
ENSP00000478688.1:n.560-2152C=
|
|
NM_000488.3:c.1060C= , LRG_577t1:c.1060C=
|
NP_000479.1:p.Arg354=
|
|
XM_005245198.2:c.916C=
|
XP_005245255.1:p.Arg306=
|
|
NM_001365052.1:c.916C=
|
NP_001351981.1:p.Arg306=
|
|
NM_000488.4:c.1060C=
MANE Select
|
NP_000479.1:p.Arg354=
|
|
NM_001365052.2:c.916C=
|
NP_001351981.1:p.Arg306=
|
|
NM_001386302.1:c.1183C=
|
NP_001373231.1:p.Arg395=
|
|
NM_001386303.1:c.1141C=
|
NP_001373232.1:p.Arg381=
|
|
NM_001386304.1:c.1039C=
|
NP_001373233.1:p.Arg347=
|
|
NM_001386305.1:c.1003C=
|
NP_001373234.1:p.Arg335=
|
|
NM_001386306.1:c.844C=
|
NP_001373235.1:p.Arg282=
|
|