ENST00000367698.4:c.880C>T
MANE Select
|
ENSP00000356671.3:p.Arg294Cys
|
|
ENST00000367698.3:c.880C>T
|
ENSP00000356671.3:p.Arg294Cys
|
|
ENST00000487183.1:n.531C>T
|
|
|
ENST00000617423.4:c.559+2039C>T
|
ENSP00000478688.1:n.559+2039C>T
|
|
NM_000488.3:c.880C>T , LRG_577t1:c.880C>T
|
NP_000479.1:p.Arg294Cys
|
|
XM_005245198.2:c.736C>T
|
XP_005245255.1:p.Arg246Cys
|
|
NM_001365052.1:c.736C>T
|
NP_001351981.1:p.Arg246Cys
|
|
NM_000488.4:c.880C>T
MANE Select
|
NP_000479.1:p.Arg294Cys
|
|
NM_001365052.2:c.736C>T
|
NP_001351981.1:p.Arg246Cys
|
|
NM_001386302.1:c.1003C>T
|
NP_001373231.1:p.Arg335Cys
|
|
NM_001386303.1:c.961C>T
|
NP_001373232.1:p.Arg321Cys
|
|
NM_001386304.1:c.859C>T
|
NP_001373233.1:p.Arg287Cys
|
|
NM_001386305.1:c.823C>T
|
NP_001373234.1:p.Arg275Cys
|
|
NM_001386306.1:c.664C>T
|
NP_001373235.1:p.Arg222Cys
|
|