ENST00000589093.6:c.1579G>A
MANE Select
|
ENSP00000466285.1:p.Gly527Arg
|
|
ENST00000589093.5:c.1579G>A
|
ENSP00000466285.1:p.Gly527Arg
|
|
ENST00000589824.6:c.1579G>A
|
ENSP00000468082.1:p.Gly527Arg
|
|
ENST00000590409.5:c.1282G>A
|
ENSP00000466582.1:p.Gly428Arg
|
|
ENST00000592953.5:c.1282G>A
|
ENSP00000468196.1:p.Gly428Arg
|
|
ENST00000593244.5:c.1579G>A
|
ENSP00000467988.1:p.Gly527Arg
|
|
NM_001297743.1:c.1282G>A
|
NP_001284672.1:p.Gly428Arg
|
|
NM_145007.3:c.1579G>A
|
NP_659444.2:p.Gly527Arg
|
|
NM_001297743.3:c.1282G>A
|
NP_001284672.1:p.Gly428Arg
|
|
NM_001385451.2:c.1579G>A
|
NP_001372380.1:p.Gly527Arg
|
|
NM_001385453.2:c.1579G>A
|
NP_001372382.1:p.Gly527Arg
|
|
NM_145007.5:c.1579G>A
|
NP_659444.2:p.Gly527Arg
|
|
NR_169620.2:n.1770G>A
|
|
|
NR_169621.2:n.2103G>A
|
|
|
NR_169622.2:n.796-7292G>A
|
|
|
NM_001394894.2:c.1579G>A
MANE Select
|
NP_001381823.1:p.Gly527Arg
|
|