ENST00000591902.6:c.153G=
|
ENSP00000468203.2:p.Glu51=
|
|
ENST00000644624.1:c.*92G=
|
ENSP00000494878.1:n.*92G=
|
|
ENST00000645214.2:c.153G=
MANE Select
|
ENSP00000494352.1:p.Glu51=
|
|
ENST00000646205.1:c.*303G=
|
ENSP00000496260.1:n.*303G=
|
|
ENST00000326575.9:c.153G=
|
ENSP00000312939.5:p.Glu51=
|
|
ENST00000406396.7:c.153G=
|
ENSP00000385083.2:p.Glu51=
|
|
ENST00000585456.1:n.163G=
|
|
|
ENST00000589530.5:n.238G=
|
|
|
ENST00000592327.1:c.153G=
|
ENSP00000467962.1:p.Glu51=
|
|
NM_002035.2:c.153G=
|
NP_002026.1:p.Glu51=
|
|
XM_005266677.1:c.153G=
|
XP_005266734.1:p.Glu51=
|
|
XM_006722433.2:c.66G=
|
XP_006722496.1:p.Glu22=
|
|
NM_002035.4:c.153G=
MANE Select
|
NP_002026.1:p.Glu51=
|
|
XM_005266677.3:c.153G=
|
XP_005266734.1:p.Glu51=
|
|
XM_017025690.2:c.-79G=
|
XP_016881179.1:n.-79G=
|
|