|
ENST00000367698.4:c.858G=
MANE Select
|
ENSP00000356671.3:p.Gln286=
|
|
|
ENST00000367698.3:c.858G=
|
ENSP00000356671.3:p.Gln286=
|
|
|
ENST00000487183.1:n.509G=
|
|
|
|
ENST00000617423.4:c.559+2017G=
|
ENSP00000478688.1:n.559+2017G=
|
|
|
NM_000488.3:c.858G= , LRG_577t1:c.858G=
|
NP_000479.1:p.Gln286=
|
|
|
XM_005245198.2:c.714G=
|
XP_005245255.1:p.Gln238=
|
|
|
NM_001365052.1:c.714G=
|
NP_001351981.1:p.Gln238=
|
|
|
NM_000488.4:c.858G=
MANE Select
|
NP_000479.1:p.Gln286=
|
|
|
NM_001365052.2:c.714G=
|
NP_001351981.1:p.Gln238=
|
|
|
NM_001386302.1:c.981G=
|
NP_001373231.1:p.Gln327=
|
|
|
NM_001386303.1:c.939G=
|
NP_001373232.1:p.Gln313=
|
|
|
NM_001386304.1:c.837G=
|
NP_001373233.1:p.Gln279=
|
|
|
NM_001386305.1:c.801G=
|
NP_001373234.1:p.Gln267=
|
|
|
NM_001386306.1:c.642G=
|
NP_001373235.1:p.Gln214=
|
|
