ENST00000355943.8:c.714G=
MANE Select
|
ENSP00000348211.3:p.Glu238=
|
|
ENST00000355943.7:c.714G=
|
ENSP00000348211.3:p.Glu238=
|
|
ENST00000447245.6:c.679-208G=
|
ENSP00000399717.2:n.679-208G=
|
|
ENST00000502462.6:n.1030G=
|
|
|
ENST00000504098.1:c.276G=
|
ENSP00000425708.1:p.Glu92=
|
|
ENST00000509432.1:c.75G=
|
ENSP00000426604.1:p.Glu25=
|
|
ENST00000513706.2:n.2314G=
|
|
|
ENST00000513807.5:c.228G=
|
ENSP00000421134.1:p.Glu76=
|
|
NM_001303249.1:c.679-208G=
|
NP_001290178.1:n.679-208G=
|
|
NM_001303250.1:c.441G=
|
NP_001290179.1:p.Glu147=
|
|
NM_138773.2:c.714G=
|
NP_620128.1:p.Glu238=
|
|
NM_001303249.2:c.679-208G=
|
NP_001290178.1:n.679-208G=
|
|
NM_001303250.2:c.441G=
|
NP_001290179.1:p.Glu147=
|
|
NM_138773.3:c.714G=
|
NP_620128.1:p.Glu238=
|
|
NR_138151.1:n.988G=
|
|
|
NM_138773.4:c.714G=
MANE Select
|
NP_620128.1:p.Glu238=
|
|
NM_001303249.3:c.679-208G=
|
NP_001290178.1:n.679-208G=
|
|
NM_001303250.3:c.441G=
|
NP_001290179.1:p.Glu147=
|
|
NR_138151.2:n.953G=
|
|
|