|
ENST00000367698.4:c.893G>T
MANE Select
|
ENSP00000356671.3:p.Gly298Val
|
|
|
ENST00000367698.3:c.893G>T
|
ENSP00000356671.3:p.Gly298Val
|
|
|
ENST00000487183.1:n.544G>T
|
|
|
|
ENST00000617423.4:c.559+2052G>T
|
ENSP00000478688.1:n.559+2052G>T
|
|
|
NM_000488.3:c.893G>T , LRG_577t1:c.893G>T
|
NP_000479.1:p.Gly298Val
|
|
|
XM_005245198.2:c.749G>T
|
XP_005245255.1:p.Gly250Val
|
|
|
NM_001365052.1:c.749G>T
|
NP_001351981.1:p.Gly250Val
|
|
|
NM_000488.4:c.893G>T
MANE Select
|
NP_000479.1:p.Gly298Val
|
|
|
NM_001365052.2:c.749G>T
|
NP_001351981.1:p.Gly250Val
|
|
|
NM_001386302.1:c.1016G>T
|
NP_001373231.1:p.Gly339Val
|
|
|
NM_001386303.1:c.974G>T
|
NP_001373232.1:p.Gly325Val
|
|
|
NM_001386304.1:c.872G>T
|
NP_001373233.1:p.Gly291Val
|
|
|
NM_001386305.1:c.836G>T
|
NP_001373234.1:p.Gly279Val
|
|
|
NM_001386306.1:c.677G>T
|
NP_001373235.1:p.Gly226Val
|
|
