ENST00000216714.8:c.258A>G
MANE Select
|
ENSP00000216714.3:p.Glu86=
|
|
ENST00000216714.7:c.258A>G
|
ENSP00000216714.3:p.Glu86=
|
|
ENST00000398030.8:c.258A>G
|
ENSP00000381111.4:p.Glu86=
|
|
ENST00000438886.1:c.107A>G
|
|
|
ENST00000553555.5:n.678A>G
|
|
|
ENST00000553681.5:c.258A>G
|
ENSP00000451327.1:p.Glu86=
|
|
ENST00000554325.1:c.*178A>G
|
ENSP00000450604.1:n.*178A>G
|
|
ENST00000554813.5:n.324A>G
|
|
|
ENST00000555306.5:n.705A>G
|
|
|
ENST00000555414.5:c.258A>G
|
ENSP00000451979.1:p.Glu86=
|
|
ENST00000555839.5:c.258A>G
|
ENSP00000452460.1:p.Glu86=
|
|
ENST00000556054.5:c.258A>G
|
ENSP00000451170.1:p.Glu86=
|
|
ENST00000557054.1:c.28-444A>G
|
ENSP00000452212.2:n.28-444A>G
|
|
ENST00000557150.5:c.207A>G
|
ENSP00000452418.1:p.Glu69=
|
|
ENST00000557159.5:n.874A>G
|
|
|
ENST00000557181.5:c.258A>G
|
ENSP00000452304.1:p.Glu86=
|
|
ENST00000557344.5:c.258A>G
|
ENSP00000452137.1:p.Glu86=
|
|
ENST00000557365.1:n.338A>G
|
|
|
ENST00000557592.5:c.207A>G
|
ENSP00000451060.1:p.Glu69=
|
|
NM_001244249.1:c.258A>G
|
NP_001231178.1:p.Glu86=
|
|
NM_001641.3:c.258A>G
|
NP_001632.2:p.Glu86=
|
|
NM_080648.2:c.258A>G
|
NP_542379.1:p.Glu86=
|
|
NM_080649.2:c.258A>G
|
NP_542380.1:p.Glu86=
|
|
XM_005267581.3:c.258A>G
|
XP_005267638.1:p.Glu86=
|
|
XM_005267582.3:c.207A>G
|
XP_005267639.1:p.Glu69=
|
|
NM_001641.4:c.258A>G
MANE Select
|
NP_001632.2:p.Glu86=
|
|
NM_001244249.2:c.258A>G
|
NP_001231178.1:p.Glu86=
|
|
NM_080648.3:c.258A>G
|
NP_542379.1:p.Glu86=
|
|
NM_080649.3:c.258A>G
|
NP_542380.1:p.Glu86=
|
|