ENST00000367698.4:c.1060C>T
MANE Select
|
ENSP00000356671.3:p.Arg354Cys
|
|
ENST00000367698.3:c.1060C>T
|
ENSP00000356671.3:p.Arg354Cys
|
|
ENST00000617423.4:c.560-2152C>T
|
ENSP00000478688.1:n.560-2152C>T
|
|
NM_000488.3:c.1060C>T , LRG_577t1:c.1060C>T
|
NP_000479.1:p.Arg354Cys
|
|
XM_005245198.2:c.916C>T
|
XP_005245255.1:p.Arg306Cys
|
|
NM_001365052.1:c.916C>T
|
NP_001351981.1:p.Arg306Cys
|
|
NM_000488.4:c.1060C>T
MANE Select
|
NP_000479.1:p.Arg354Cys
|
|
NM_001365052.2:c.916C>T
|
NP_001351981.1:p.Arg306Cys
|
|
NM_001386302.1:c.1183C>T
|
NP_001373231.1:p.Arg395Cys
|
|
NM_001386303.1:c.1141C>T
|
NP_001373232.1:p.Arg381Cys
|
|
NM_001386304.1:c.1039C>T
|
NP_001373233.1:p.Arg347Cys
|
|
NM_001386305.1:c.1003C>T
|
NP_001373234.1:p.Arg335Cys
|
|
NM_001386306.1:c.844C>T
|
NP_001373235.1:p.Arg282Cys
|
|