ENST00000367698.4:c.857A>G
MANE Select
|
ENSP00000356671.3:p.Gln286Arg
|
|
ENST00000367698.3:c.857A>G
|
ENSP00000356671.3:p.Gln286Arg
|
|
ENST00000487183.1:n.508A>G
|
|
|
ENST00000617423.4:c.559+2016A>G
|
ENSP00000478688.1:n.559+2016A>G
|
|
NM_000488.3:c.857A>G , LRG_577t1:c.857A>G
|
NP_000479.1:p.Gln286Arg
|
|
XM_005245198.2:c.713A>G
|
XP_005245255.1:p.Gln238Arg
|
|
NM_001365052.1:c.713A>G
|
NP_001351981.1:p.Gln238Arg
|
|
NM_000488.4:c.857A>G
MANE Select
|
NP_000479.1:p.Gln286Arg
|
|
NM_001365052.2:c.713A>G
|
NP_001351981.1:p.Gln238Arg
|
|
NM_001386302.1:c.980A>G
|
NP_001373231.1:p.Gln327Arg
|
|
NM_001386303.1:c.938A>G
|
NP_001373232.1:p.Gln313Arg
|
|
NM_001386304.1:c.836A>G
|
NP_001373233.1:p.Gln279Arg
|
|
NM_001386305.1:c.800A>G
|
NP_001373234.1:p.Gln267Arg
|
|
NM_001386306.1:c.641A>G
|
NP_001373235.1:p.Gln214Arg
|
|