ENST00000367698.4:c.827G>A
MANE Select
|
ENSP00000356671.3:p.Gly276Glu
|
|
ENST00000367698.3:c.827G>A
|
ENSP00000356671.3:p.Gly276Glu
|
|
ENST00000487183.1:n.478G>A
|
|
|
ENST00000617423.4:c.559+1986G>A
|
ENSP00000478688.1:n.559+1986G>A
|
|
NM_000488.3:c.827G>A , LRG_577t1:c.827G>A
|
NP_000479.1:p.Gly276Glu
|
|
XM_005245198.2:c.683G>A
|
XP_005245255.1:p.Gly228Glu
|
|
NM_001365052.1:c.683G>A
|
NP_001351981.1:p.Gly228Glu
|
|
NM_000488.4:c.827G>A
MANE Select
|
NP_000479.1:p.Gly276Glu
|
|
NM_001365052.2:c.683G>A
|
NP_001351981.1:p.Gly228Glu
|
|
NM_001386302.1:c.950G>A
|
NP_001373231.1:p.Gly317Glu
|
|
NM_001386303.1:c.908G>A
|
NP_001373232.1:p.Gly303Glu
|
|
NM_001386304.1:c.806G>A
|
NP_001373233.1:p.Gly269Glu
|
|
NM_001386305.1:c.770G>A
|
NP_001373234.1:p.Gly257Glu
|
|
NM_001386306.1:c.611G>A
|
NP_001373235.1:p.Gly204Glu
|
|