ENST00000367698.4:c.1066C>T
MANE Select
|
ENSP00000356671.3:p.Arg356Cys
|
|
ENST00000367698.3:c.1066C>T
|
ENSP00000356671.3:p.Arg356Cys
|
|
ENST00000617423.4:c.560-2146C>T
|
ENSP00000478688.1:n.560-2146C>T
|
|
NM_000488.3:c.1066C>T , LRG_577t1:c.1066C>T
|
NP_000479.1:p.Arg356Cys
|
|
XM_005245198.2:c.922C>T
|
XP_005245255.1:p.Arg308Cys
|
|
NM_001365052.1:c.922C>T
|
NP_001351981.1:p.Arg308Cys
|
|
NM_000488.4:c.1066C>T
MANE Select
|
NP_000479.1:p.Arg356Cys
|
|
NM_001365052.2:c.922C>T
|
NP_001351981.1:p.Arg308Cys
|
|
NM_001386302.1:c.1189C>T
|
NP_001373231.1:p.Arg397Cys
|
|
NM_001386303.1:c.1147C>T
|
NP_001373232.1:p.Arg383Cys
|
|
NM_001386304.1:c.1045C>T
|
NP_001373233.1:p.Arg349Cys
|
|
NM_001386305.1:c.1009C>T
|
NP_001373234.1:p.Arg337Cys
|
|
NM_001386306.1:c.850C>T
|
NP_001373235.1:p.Arg284Cys
|
|