ENST00000682568.1:n.1792G>A
|
|
|
ENST00000682617.1:c.1852G>A
|
ENSP00000507912.1:p.Glu618Lys
|
|
ENST00000682826.1:c.*1028G>A
|
ENSP00000507274.1:n.*1028G>A
|
|
ENST00000682909.1:n.3754G>A
|
|
|
ENST00000683277.1:n.3359G>A
|
|
|
ENST00000683407.1:n.1722G>A
|
|
|
ENST00000683962.1:c.*1408G>A
|
ENSP00000506854.1:n.*1408G>A
|
|
ENST00000311895.8:c.1714G>A
MANE Select
|
ENSP00000310520.7:p.Glu572Lys
|
|
ENST00000311895.7:c.1714G>A
|
ENSP00000310520.7:p.Glu572Lys
|
|
ENST00000389138.7:n.991G>A
|
|
|
NM_005236.2:c.1714G>A , LRG_463t1:c.1714G>A
|
NP_005227.1:p.Glu572Lys
|
|
XM_011522424.1:c.1852G>A
|
XP_011520726.1:p.Glu618Lys
|
|
XM_011522425.1:c.1171G>A
|
XP_011520727.1:p.Glu391Lys
|
|
XM_011522426.1:c.925G>A
|
XP_011520728.1:p.Glu309Lys
|
|
XM_011522427.1:c.364G>A
|
XP_011520729.1:p.Glu122Lys
|
|
XR_932805.1:n.1873G>A
|
|
|
XM_011522424.3:c.1852G>A
|
XP_011520726.1:p.Glu618Lys
|
|
XM_017023043.2:c.925G>A
|
XP_016878532.1:p.Glu309Lys
|
|
NM_005236.3:c.1714G>A
MANE Select
|
NP_005227.1:p.Glu572Lys
|
|