|
ENST00000367698.4:c.923G>A
MANE Select
|
ENSP00000356671.3:p.Gly308Asp
|
|
|
ENST00000367698.3:c.923G>A
|
ENSP00000356671.3:p.Gly308Asp
|
|
|
ENST00000487183.1:n.574G>A
|
|
|
|
ENST00000617423.4:c.559+2082G>A
|
ENSP00000478688.1:n.559+2082G>A
|
|
|
NM_000488.3:c.923G>A , LRG_577t1:c.923G>A
|
NP_000479.1:p.Gly308Asp
|
|
|
XM_005245198.2:c.779G>A
|
XP_005245255.1:p.Gly260Asp
|
|
|
NM_001365052.1:c.779G>A
|
NP_001351981.1:p.Gly260Asp
|
|
|
NM_000488.4:c.923G>A
MANE Select
|
NP_000479.1:p.Gly308Asp
|
|
|
NM_001365052.2:c.779G>A
|
NP_001351981.1:p.Gly260Asp
|
|
|
NM_001386302.1:c.1046G>A
|
NP_001373231.1:p.Gly349Asp
|
|
|
NM_001386303.1:c.1004G>A
|
NP_001373232.1:p.Gly335Asp
|
|
|
NM_001386304.1:c.902G>A
|
NP_001373233.1:p.Gly301Asp
|
|
|
NM_001386305.1:c.866G>A
|
NP_001373234.1:p.Gly289Asp
|
|
|
NM_001386306.1:c.707G>A
|
NP_001373235.1:p.Gly236Asp
|
|
