ENST00000355943.8:c.1149T>A
MANE Select
|
ENSP00000348211.3:p.Phe383Leu
|
|
ENST00000355943.7:c.1149T>A
|
ENSP00000348211.3:p.Phe383Leu
|
|
ENST00000447245.6:c.906T>A
|
ENSP00000399717.2:p.Phe302Leu
|
|
ENST00000504098.1:c.711T>A
|
ENSP00000425708.1:p.Phe237Leu
|
|
ENST00000509432.1:c.510T>A
|
ENSP00000426604.1:p.Phe170Leu
|
|
ENST00000513706.2:n.2749T>A
|
|
|
ENST00000513807.5:c.663T>A
|
ENSP00000421134.1:p.Phe221Leu
|
|
NM_001303249.1:c.906T>A
|
NP_001290178.1:p.Phe302Leu
|
|
NM_001303250.1:c.876T>A
|
NP_001290179.1:p.Phe292Leu
|
|
NM_138773.2:c.1149T>A
|
NP_620128.1:p.Phe383Leu
|
|
NM_001303249.2:c.906T>A
|
NP_001290178.1:p.Phe302Leu
|
|
NM_001303250.2:c.876T>A
|
NP_001290179.1:p.Phe292Leu
|
|
NM_138773.3:c.1149T>A
|
NP_620128.1:p.Phe383Leu
|
|
NR_138151.1:n.1423T>A
|
|
|
NM_138773.4:c.1149T>A
MANE Select
|
NP_620128.1:p.Phe383Leu
|
|
NM_001303249.3:c.906T>A
|
NP_001290178.1:p.Phe302Leu
|
|
NM_001303250.3:c.876T>A
|
NP_001290179.1:p.Phe292Leu
|
|
NR_138151.2:n.1388T>A
|
|
|