ENST00000367698.4:c.771G>T
MANE Select
|
ENSP00000356671.3:p.Trp257Cys
|
|
ENST00000367698.3:c.771G>T
|
ENSP00000356671.3:p.Trp257Cys
|
|
ENST00000487183.1:n.422G>T
|
|
|
ENST00000617423.4:c.559+1930G>T
|
ENSP00000478688.1:n.559+1930G>T
|
|
NM_000488.3:c.771G>T , LRG_577t1:c.771G>T
|
NP_000479.1:p.Trp257Cys
|
|
XM_005245198.2:c.627G>T
|
XP_005245255.1:p.Trp209Cys
|
|
NM_001365052.1:c.627G>T
|
NP_001351981.1:p.Trp209Cys
|
|
NM_000488.4:c.771G>T
MANE Select
|
NP_000479.1:p.Trp257Cys
|
|
NM_001365052.2:c.627G>T
|
NP_001351981.1:p.Trp209Cys
|
|
NM_001386302.1:c.894G>T
|
NP_001373231.1:p.Trp298Cys
|
|
NM_001386303.1:c.852G>T
|
NP_001373232.1:p.Trp284Cys
|
|
NM_001386304.1:c.750G>T
|
NP_001373233.1:p.Trp250Cys
|
|
NM_001386305.1:c.763-49G>T
|
NP_001373234.1:n.763-49G>T
|
|
NM_001386306.1:c.555G>T
|
NP_001373235.1:p.Trp185Cys
|
|