|
ENST00000367698.4:c.830A>T
MANE Select
|
ENSP00000356671.3:p.Glu277Val
|
|
|
ENST00000367698.3:c.830A>T
|
ENSP00000356671.3:p.Glu277Val
|
|
|
ENST00000487183.1:n.481A>T
|
|
|
|
ENST00000617423.4:c.559+1989A>T
|
ENSP00000478688.1:n.559+1989A>T
|
|
|
NM_000488.3:c.830A>T , LRG_577t1:c.830A>T
|
NP_000479.1:p.Glu277Val
|
|
|
XM_005245198.2:c.686A>T
|
XP_005245255.1:p.Glu229Val
|
|
|
NM_001365052.1:c.686A>T
|
NP_001351981.1:p.Glu229Val
|
|
|
NM_000488.4:c.830A>T
MANE Select
|
NP_000479.1:p.Glu277Val
|
|
|
NM_001365052.2:c.686A>T
|
NP_001351981.1:p.Glu229Val
|
|
|
NM_001386302.1:c.953A>T
|
NP_001373231.1:p.Glu318Val
|
|
|
NM_001386303.1:c.911A>T
|
NP_001373232.1:p.Glu304Val
|
|
|
NM_001386304.1:c.809A>T
|
NP_001373233.1:p.Glu270Val
|
|
|
NM_001386305.1:c.773A>T
|
NP_001373234.1:p.Glu258Val
|
|
|
NM_001386306.1:c.614A>T
|
NP_001373235.1:p.Glu205Val
|
|
