ENST00000352480.10:c.586G=
MANE Select
|
ENSP00000253004.6:p.Glu196=
|
|
ENST00000352480.9:c.586G=
|
ENSP00000253004.6:p.Glu196=
|
|
ENST00000372393.7:c.586G=
|
ENSP00000361469.2:p.Glu196=
|
|
ENST00000372394.5:c.586G=
|
ENSP00000361471.1:p.Glu196=
|
|
ENST00000422569.5:c.586G=
|
ENSP00000394212.1:p.Glu196=
|
|
ENST00000443588.1:c.529G=
|
ENSP00000397785.1:p.Glu177=
|
|
ENST00000467695.5:n.295G=
|
|
|
ENST00000493984.6:n.417G=
|
|
|
NM_000050.4:c.586G=
|
NP_000041.2:p.Glu196=
|
|
NM_054012.3:c.586G=
|
NP_446464.1:p.Glu196=
|
|
XM_005272200.2:c.586G=
|
XP_005272257.1:p.Glu196=
|
|
XM_011518705.1:c.700G=
|
XP_011517007.1:p.Glu234=
|
|
XM_005272200.3:c.586G=
|
XP_005272257.1:p.Glu196=
|
|
XM_011518705.2:c.700G=
|
XP_011517007.1:p.Glu234=
|
|
XM_017014729.1:c.682G=
|
XP_016870218.1:p.Glu228=
|
|
NM_054012.4:c.586G=
MANE Select
|
NP_446464.1:p.Glu196=
|
|