|
ENST00000367698.4:c.763G=
MANE Select
|
ENSP00000356671.3:p.Gly255=
|
|
|
ENST00000367698.3:c.763G=
|
ENSP00000356671.3:p.Gly255=
|
|
|
ENST00000487183.1:n.414G=
|
|
|
|
ENST00000617423.4:c.559+1922G=
|
ENSP00000478688.1:n.559+1922G=
|
|
|
NM_000488.3:c.763G= , LRG_577t1:c.763G=
|
NP_000479.1:p.Gly255=
|
|
|
XM_005245198.2:c.619G=
|
XP_005245255.1:p.Gly207=
|
|
|
NM_001365052.1:c.619G=
|
NP_001351981.1:p.Gly207=
|
|
|
NM_000488.4:c.763G=
MANE Select
|
NP_000479.1:p.Gly255=
|
|
|
NM_001365052.2:c.619G=
|
NP_001351981.1:p.Gly207=
|
|
|
NM_001386302.1:c.886G=
|
NP_001373231.1:p.Gly296=
|
|
|
NM_001386303.1:c.844G=
|
NP_001373232.1:p.Gly282=
|
|
|
NM_001386304.1:c.742G=
|
NP_001373233.1:p.Gly248=
|
|
|
NM_001386305.1:c.763-57G=
|
NP_001373234.1:n.763-57G=
|
|
|
NM_001386306.1:c.547G=
|
NP_001373235.1:p.Gly183=
|
|
