ENST00000474627.8:c.721G=
MANE Select
|
ENSP00000417190.2:p.Glu241=
|
|
ENST00000462733.5:c.*138G=
|
ENSP00000463920.1:n.*138G=
|
|
ENST00000465337.2:n.580G=
|
|
|
ENST00000467560.5:n.131G=
|
|
|
ENST00000469327.5:n.631G=
|
|
|
ENST00000474627.7:c.721G=
|
ENSP00000417190.2:p.Glu241=
|
|
ENST00000488753.1:n.516G=
|
|
|
ENST00000496852.5:n.1226G=
|
|
|
ENST00000581698.1:c.49-2448G=
|
|
|
ENST00000584205.5:c.*33+3490G=
|
ENSP00000462899.1:n.*33+3490G=
|
|
ENST00000585101.5:c.*33+3490G=
|
ENSP00000463861.1:n.*33+3490G=
|
|
NM_145691.3:c.721G=
|
NP_663729.1:p.Glu241=
|
|
XM_005256848.2:c.721G=
|
XP_005256905.1:p.Glu241=
|
|
XM_011524062.1:c.721G=
|
XP_011522364.1:p.Glu241=
|
|
XM_011524063.1:c.721G=
|
XP_011522365.1:p.Glu241=
|
|
XM_011524064.1:c.421G=
|
XP_011522366.1:p.Glu141=
|
|
XM_011524065.1:c.721G=
|
XP_011522367.1:p.Glu241=
|
|
XM_011524066.1:c.184G=
|
XP_011522368.1:p.Glu62=
|
|
XM_005256848.4:c.721G=
|
XP_005256905.1:p.Glu241=
|
|
XM_011524065.2:c.721G=
|
XP_011522367.1:p.Glu241=
|
|
XM_017025302.1:c.421G=
|
XP_016880791.1:p.Glu141=
|
|
XM_017025303.1:c.421G=
|
XP_016880792.1:p.Glu141=
|
|
XR_001752677.2:n.1118G=
|
|
|
NM_145691.4:c.721G=
MANE Select
|
NP_663729.1:p.Glu241=
|
|