ENST00000355943.8:c.1148T>A
MANE Select
|
ENSP00000348211.3:p.Phe383Tyr
|
|
ENST00000355943.7:c.1148T>A
|
ENSP00000348211.3:p.Phe383Tyr
|
|
ENST00000447245.6:c.905T>A
|
ENSP00000399717.2:p.Phe302Tyr
|
|
ENST00000504098.1:c.710T>A
|
ENSP00000425708.1:p.Phe237Tyr
|
|
ENST00000509432.1:c.509T>A
|
ENSP00000426604.1:p.Phe170Tyr
|
|
ENST00000513706.2:n.2748T>A
|
|
|
ENST00000513807.5:c.662T>A
|
ENSP00000421134.1:p.Phe221Tyr
|
|
NM_001303249.1:c.905T>A
|
NP_001290178.1:p.Phe302Tyr
|
|
NM_001303250.1:c.875T>A
|
NP_001290179.1:p.Phe292Tyr
|
|
NM_138773.2:c.1148T>A
|
NP_620128.1:p.Phe383Tyr
|
|
NM_001303249.2:c.905T>A
|
NP_001290178.1:p.Phe302Tyr
|
|
NM_001303250.2:c.875T>A
|
NP_001290179.1:p.Phe292Tyr
|
|
NM_138773.3:c.1148T>A
|
NP_620128.1:p.Phe383Tyr
|
|
NR_138151.1:n.1422T>A
|
|
|
NM_138773.4:c.1148T>A
MANE Select
|
NP_620128.1:p.Phe383Tyr
|
|
NM_001303249.3:c.905T>A
|
NP_001290178.1:p.Phe302Tyr
|
|
NM_001303250.3:c.875T>A
|
NP_001290179.1:p.Phe292Tyr
|
|
NR_138151.2:n.1387T>A
|
|
|