|
ENST00000367698.4:c.880C=
MANE Select
|
ENSP00000356671.3:p.Arg294=
|
|
|
ENST00000367698.3:c.880C=
|
ENSP00000356671.3:p.Arg294=
|
|
|
ENST00000487183.1:n.531C=
|
|
|
|
ENST00000617423.4:c.559+2039C=
|
ENSP00000478688.1:n.559+2039C=
|
|
|
NM_000488.3:c.880C= , LRG_577t1:c.880C=
|
NP_000479.1:p.Arg294=
|
|
|
XM_005245198.2:c.736C=
|
XP_005245255.1:p.Arg246=
|
|
|
NM_001365052.1:c.736C=
|
NP_001351981.1:p.Arg246=
|
|
|
NM_000488.4:c.880C=
MANE Select
|
NP_000479.1:p.Arg294=
|
|
|
NM_001365052.2:c.736C=
|
NP_001351981.1:p.Arg246=
|
|
|
NM_001386302.1:c.1003C=
|
NP_001373231.1:p.Arg335=
|
|
|
NM_001386303.1:c.961C=
|
NP_001373232.1:p.Arg321=
|
|
|
NM_001386304.1:c.859C=
|
NP_001373233.1:p.Arg287=
|
|
|
NM_001386305.1:c.823C=
|
NP_001373234.1:p.Arg275=
|
|
|
NM_001386306.1:c.664C=
|
NP_001373235.1:p.Arg222=
|
|
