ENST00000367698.4:c.167G>A
MANE Select
|
ENSP00000356671.3:p.Arg56His
|
|
ENST00000367698.3:c.167G>A
|
ENSP00000356671.3:p.Arg56His
|
|
ENST00000494024.1:n.393G>A
|
|
|
ENST00000617423.4:c.167G>A
|
ENSP00000478688.1:p.Arg56His
|
|
NM_000488.3:c.167G>A , LRG_577t1:c.167G>A
|
NP_000479.1:p.Arg56His
|
|
XM_005245198.2:c.23G>A
|
XP_005245255.1:p.Arg8His
|
|
NM_001365052.1:c.23G>A
|
NP_001351981.1:p.Arg8His
|
|
NM_000488.4:c.167G>A
MANE Select
|
NP_000479.1:p.Arg56His
|
|
NM_001365052.2:c.23G>A
|
NP_001351981.1:p.Arg8His
|
|
NM_001386302.1:c.167G>A
|
NP_001373231.1:p.Arg56His
|
|
NM_001386303.1:c.248G>A
|
NP_001373232.1:p.Arg83His
|
|
NM_001386304.1:c.167G>A
|
NP_001373233.1:p.Arg56His
|
|
NM_001386305.1:c.167G>A
|
NP_001373234.1:p.Arg56His
|
|
NM_001386306.1:c.167G>A
|
NP_001373235.1:p.Arg56His
|
|