ENST00000682568.1:n.1657G>T
|
|
|
ENST00000682617.1:c.1717G>T
|
ENSP00000507912.1:p.Glu573Ter
|
|
ENST00000682826.1:c.*893G>T
|
ENSP00000507274.1:n.*893G>T
|
|
ENST00000682909.1:n.3619G>T
|
|
|
ENST00000683277.1:n.3224G>T
|
|
|
ENST00000683407.1:n.1587G>T
|
|
|
ENST00000683962.1:c.*1273G>T
|
ENSP00000506854.1:n.*1273G>T
|
|
ENST00000311895.8:c.1579G>T
MANE Select
|
ENSP00000310520.7:p.Glu527Ter
|
|
ENST00000311895.7:c.1579G>T
|
ENSP00000310520.7:p.Glu527Ter
|
|
ENST00000389138.7:n.856G>T
|
|
|
NM_005236.2:c.1579G>T , LRG_463t1:c.1579G>T
|
NP_005227.1:p.Glu527Ter
|
|
XM_011522424.1:c.1717G>T
|
XP_011520726.1:p.Glu573Ter
|
|
XM_011522425.1:c.1036G>T
|
XP_011520727.1:p.Glu346Ter
|
|
XM_011522426.1:c.790G>T
|
XP_011520728.1:p.Glu264Ter
|
|
XM_011522427.1:c.229G>T
|
XP_011520729.1:p.Glu77Ter
|
|
XR_932805.1:n.1738G>T
|
|
|
XM_011522424.3:c.1717G>T
|
XP_011520726.1:p.Glu573Ter
|
|
XM_017023043.2:c.790G>T
|
XP_016878532.1:p.Glu264Ter
|
|
NM_005236.3:c.1579G>T
MANE Select
|
NP_005227.1:p.Glu527Ter
|
|