ENST00000367698.4:c.777A>G
MANE Select
|
ENSP00000356671.3:p.Ser259=
|
|
ENST00000367698.3:c.777A>G
|
ENSP00000356671.3:p.Ser259=
|
|
ENST00000487183.1:n.428A>G
|
|
|
ENST00000617423.4:c.559+1936A>G
|
ENSP00000478688.1:n.559+1936A>G
|
|
NM_000488.3:c.777A>G , LRG_577t1:c.777A>G
|
NP_000479.1:p.Ser259=
|
|
XM_005245198.2:c.633A>G
|
XP_005245255.1:p.Ser211=
|
|
NM_001365052.1:c.633A>G
|
NP_001351981.1:p.Ser211=
|
|
NM_000488.4:c.777A>G
MANE Select
|
NP_000479.1:p.Ser259=
|
|
NM_001365052.2:c.633A>G
|
NP_001351981.1:p.Ser211=
|
|
NM_001386302.1:c.900A>G
|
NP_001373231.1:p.Ser300=
|
|
NM_001386303.1:c.858A>G
|
NP_001373232.1:p.Ser286=
|
|
NM_001386304.1:c.756A>G
|
NP_001373233.1:p.Ser252=
|
|
NM_001386305.1:c.763-43A>G
|
NP_001373234.1:n.763-43A>G
|
|
NM_001386306.1:c.561A>G
|
NP_001373235.1:p.Ser187=
|
|