ENST00000474627.8:c.633T>G
MANE Select
|
ENSP00000417190.2:p.Ala211=
|
|
ENST00000462733.5:c.*50T>G
|
ENSP00000463920.1:n.*50T>G
|
|
ENST00000465337.2:n.492T>G
|
|
|
ENST00000467560.5:n.43T>G
|
|
|
ENST00000469327.5:n.543T>G
|
|
|
ENST00000474627.7:c.633T>G
|
ENSP00000417190.2:p.Ala211=
|
|
ENST00000488753.1:n.428T>G
|
|
|
ENST00000496852.5:n.1138T>G
|
|
|
ENST00000581698.1:c.49-2536T>G
|
|
|
ENST00000584205.5:c.*33+3402T>G
|
ENSP00000462899.1:n.*33+3402T>G
|
|
ENST00000585101.5:c.*33+3402T>G
|
ENSP00000463861.1:n.*33+3402T>G
|
|
NM_145691.3:c.633T>G
|
NP_663729.1:p.Ala211=
|
|
XM_005256848.2:c.633T>G
|
XP_005256905.1:p.Ala211=
|
|
XM_011524062.1:c.633T>G
|
XP_011522364.1:p.Ala211=
|
|
XM_011524063.1:c.633T>G
|
XP_011522365.1:p.Ala211=
|
|
XM_011524064.1:c.333T>G
|
XP_011522366.1:p.Ala111=
|
|
XM_011524065.1:c.633T>G
|
XP_011522367.1:p.Ala211=
|
|
XM_011524066.1:c.96T>G
|
XP_011522368.1:p.Ala32=
|
|
XR_934116.1:n.1031T>G
|
|
|
XM_005256848.4:c.633T>G
|
XP_005256905.1:p.Ala211=
|
|
XM_011524065.2:c.633T>G
|
XP_011522367.1:p.Ala211=
|
|
XM_017025302.1:c.333T>G
|
XP_016880791.1:p.Ala111=
|
|
XM_017025303.1:c.333T>G
|
XP_016880792.1:p.Ala111=
|
|
XR_001752677.2:n.1030T>G
|
|
|
NM_145691.4:c.633T>G
MANE Select
|
NP_663729.1:p.Ala211=
|
|