ENST00000620041.5:c.433G>T
(FTH1)
|
ENSP00000484477.1:p.Ala145Ser
|
|
ENST00000273550.12:c.433G>T
(FTH1)
MANE Select
|
ENSP00000273550.7:p.Ala145Ser
|
|
ENST00000273550.11:c.433G>T
(FTH1)
|
ENSP00000273550.7:p.Ala145Ser
|
|
ENST00000449131.6:c.*1697C>A
(BEST1)
|
ENSP00000399709.2:n.*1697C>A
|
|
ENST00000526640.5:c.343G>T
(FTH1)
|
ENSP00000433321.1:p.Ala115Ser
|
|
ENST00000529191.5:c.114+2466G>T
(FTH1)
|
ENSP00000431659.1:n.114+2466G>T
|
|
ENST00000529631.5:c.114+2466G>T
(FTH1)
|
ENSP00000431575.1:n.114+2466G>T
|
|
ENST00000530019.5:c.261+523G>T
(FTH1)
|
ENSP00000433470.1:n.261+523G>T
|
|
ENST00000532601.1:c.223G>T
(FTH1)
|
ENSP00000435111.1:p.Ala75Ser
|
|
ENST00000532829.5:c.*138G>T
(FTH1)
|
ENSP00000432223.1:n.*138G>T
|
|
ENST00000533138.1:n.877G>T
(FTH1)
|
|
|
ENST00000534180.1:c.*342G>T
(FTH1)
|
ENSP00000434403.1:n.*342G>T
|
|
ENST00000534719.1:n.689G>T
(FTH1)
|
|
|
ENST00000620041.4:c.433G>T
(FTH1)
|
ENSP00000484477.1:p.Ala145Ser
|
|
NM_002032.2:c.433G>T
(FTH1)
|
NP_002023.2:p.Ala145Ser
|
|
NM_002032.3:c.433G>T
(FTH1)
MANE Select
|
NP_002023.2:p.Ala145Ser
|
|
NM_001139443.2:c.*1697C>A
(BEST1)
|
NP_001132915.1:n.*1697C>A
|
|
NM_001363591.2:c.*1697C>A
(BEST1)
|
NP_001350520.1:n.*1697C>A
|
|
NM_001363593.2:c.*1697C>A
(BEST1)
|
NP_001350522.1:n.*1697C>A
|
|