ENST00000682568.1:n.1750C>G
|
|
|
ENST00000682617.1:c.1810C>G
|
ENSP00000507912.1:p.Leu604Val
|
|
ENST00000682826.1:c.*986C>G
|
ENSP00000507274.1:n.*986C>G
|
|
ENST00000682909.1:n.3712C>G
|
|
|
ENST00000683277.1:n.3317C>G
|
|
|
ENST00000683407.1:n.1680C>G
|
|
|
ENST00000683962.1:c.*1366C>G
|
ENSP00000506854.1:n.*1366C>G
|
|
ENST00000311895.8:c.1672C>G
MANE Select
|
ENSP00000310520.7:p.Leu558Val
|
|
ENST00000311895.7:c.1672C>G
|
ENSP00000310520.7:p.Leu558Val
|
|
ENST00000389138.7:n.949C>G
|
|
|
NM_005236.2:c.1672C>G , LRG_463t1:c.1672C>G
|
NP_005227.1:p.Leu558Val
|
|
XM_011522424.1:c.1810C>G
|
XP_011520726.1:p.Leu604Val
|
|
XM_011522425.1:c.1129C>G
|
XP_011520727.1:p.Leu377Val
|
|
XM_011522426.1:c.883C>G
|
XP_011520728.1:p.Leu295Val
|
|
XM_011522427.1:c.322C>G
|
XP_011520729.1:p.Leu108Val
|
|
XR_932805.1:n.1831C>G
|
|
|
XM_011522424.3:c.1810C>G
|
XP_011520726.1:p.Leu604Val
|
|
XM_017023043.2:c.883C>G
|
XP_016878532.1:p.Leu295Val
|
|
NM_005236.3:c.1672C>G
MANE Select
|
NP_005227.1:p.Leu558Val
|
|