ENST00000368985.8:c.916G=
MANE Select
|
ENSP00000357981.3:p.Glu306=
|
|
ENST00000448301.7:c.688G=
|
ENSP00000408414.2:p.Glu230=
|
|
ENST00000472977.7:c.916G=
|
ENSP00000475176.2:p.Glu306=
|
|
ENST00000483930.2:c.*110G=
|
ENSP00000475812.2:n.*110G=
|
|
ENST00000607427.2:c.916G=
|
ENSP00000475557.2:p.Glu306=
|
|
ENST00000679512.1:c.813G=
|
ENSP00000505113.1:p.Val271=
|
|
ENST00000679898.1:c.643G=
|
ENSP00000505326.1:p.Glu215=
|
|
ENST00000680288.1:c.766G=
|
ENSP00000506001.1:p.Glu256=
|
|
ENST00000680311.1:c.647G=
|
ENSP00000505020.1:p.Ter216=
|
|
ENST00000680471.1:c.*87G=
|
ENSP00000506603.1:n.*87G=
|
|
ENST00000680664.1:c.739G=
|
ENSP00000506248.1:p.Glu247=
|
|
ENST00000680931.1:c.*266G=
|
ENSP00000504934.1:n.*266G=
|
|
ENST00000681357.1:n.306G=
|
|
|
ENST00000681444.1:c.916G=
|
ENSP00000505359.1:p.Glu306=
|
|
ENST00000368985.7:c.916G=
|
ENSP00000357981.3:p.Glu306=
|
|
ENST00000448301.6:c.766G=
|
ENSP00000408414.1:p.Glu256=
|
|
ENST00000472977.6:c.209G=
|
|
|
ENST00000483930.1:c.464G=
|
ENSP00000475812.1:n.464G=
|
|
NM_001199739.1:c.766G=
|
NP_001186668.1:p.Glu256=
|
|
NM_004079.4:c.916G=
|
NP_004070.3:p.Glu306=
|
|
NM_004079.5:c.916G=
MANE Select
|
NP_004070.3:p.Glu306=
|
|
NM_001199739.2:c.766G=
|
NP_001186668.1:p.Glu256=
|
|