ENST00000682617.1:c.2045A>G
|
ENSP00000507912.1:p.Glu682Gly
|
|
ENST00000683962.1:c.*1601A>G
|
ENSP00000506854.1:n.*1601A>G
|
|
ENST00000311895.8:c.1907A>G
MANE Select
|
ENSP00000310520.7:p.Glu636Gly
|
|
ENST00000311895.7:c.1907A>G
|
ENSP00000310520.7:p.Glu636Gly
|
|
ENST00000389138.7:n.1184A>G
|
|
|
ENST00000462862.1:c.220A>G
|
ENSP00000461322.1:n.220A>G
|
|
NM_005236.2:c.1907A>G , LRG_463t1:c.1907A>G
|
NP_005227.1:p.Glu636Gly
|
|
XM_011522424.1:c.2045A>G
|
XP_011520726.1:p.Glu682Gly
|
|
XM_011522425.1:c.1364A>G
|
XP_011520727.1:p.Glu455Gly
|
|
XM_011522426.1:c.1118A>G
|
XP_011520728.1:p.Glu373Gly
|
|
XM_011522427.1:c.557A>G
|
XP_011520729.1:p.Glu186Gly
|
|
XR_932805.1:n.2066A>G
|
|
|
XM_011522424.3:c.2045A>G
|
XP_011520726.1:p.Glu682Gly
|
|
XM_017023043.2:c.1118A>G
|
XP_016878532.1:p.Glu373Gly
|
|
NM_005236.3:c.1907A>G
MANE Select
|
NP_005227.1:p.Glu636Gly
|
|