|
ENST00000367698.4:c.828A>T
MANE Select
|
ENSP00000356671.3:p.Gly276=
|
|
|
ENST00000367698.3:c.828A>T
|
ENSP00000356671.3:p.Gly276=
|
|
|
ENST00000487183.1:n.479A>T
|
|
|
|
ENST00000617423.4:c.559+1987A>T
|
ENSP00000478688.1:n.559+1987A>T
|
|
|
NM_000488.3:c.828A>T , LRG_577t1:c.828A>T
|
NP_000479.1:p.Gly276=
|
|
|
XM_005245198.2:c.684A>T
|
XP_005245255.1:p.Gly228=
|
|
|
NM_001365052.1:c.684A>T
|
NP_001351981.1:p.Gly228=
|
|
|
NM_000488.4:c.828A>T
MANE Select
|
NP_000479.1:p.Gly276=
|
|
|
NM_001365052.2:c.684A>T
|
NP_001351981.1:p.Gly228=
|
|
|
NM_001386302.1:c.951A>T
|
NP_001373231.1:p.Gly317=
|
|
|
NM_001386303.1:c.909A>T
|
NP_001373232.1:p.Gly303=
|
|
|
NM_001386304.1:c.807A>T
|
NP_001373233.1:p.Gly269=
|
|
|
NM_001386305.1:c.771A>T
|
NP_001373234.1:p.Gly257=
|
|
|
NM_001386306.1:c.612A>T
|
NP_001373235.1:p.Gly204=
|
|
