ENST00000447944.7:c.492G=
MANE Select
|
ENSP00000400646.2:p.Glu164=
|
|
ENST00000260604.8:c.492G=
|
ENSP00000260604.4:p.Glu164=
|
|
ENST00000415374.5:c.492G=
|
ENSP00000393953.1:p.Glu164=
|
|
ENST00000429805.1:c.*140G=
|
ENSP00000411994.1:n.*140G=
|
|
ENST00000447944.6:c.492G=
|
ENSP00000400646.2:p.Glu164=
|
|
NM_033109.4:c.492G=
|
NP_149100.2:p.Glu164=
|
|
XM_005264629.1:c.252G=
|
XP_005264686.1:p.Glu84=
|
|
XM_011533142.1:c.492G=
|
XP_011531444.1:p.Glu164=
|
|
XM_005264629.2:c.252G=
|
XP_005264686.1:p.Glu84=
|
|
XM_017005172.1:c.252G=
|
XP_016860661.1:p.Glu84=
|
|
XR_001739010.1:n.522G=
|
|
|
NM_033109.5:c.492G=
MANE Select
|
NP_149100.2:p.Glu164=
|
|