ENST00000620041.5:c.*4T>C
(FTH1)
|
ENSP00000484477.1:n.*4T>C
|
|
ENST00000273550.12:c.*4T>C
(FTH1)
MANE Select
|
ENSP00000273550.7:n.*4T>C
|
|
ENST00000273550.11:c.*4T>C
(FTH1)
|
ENSP00000273550.7:n.*4T>C
|
|
ENST00000449131.6:c.*1574A>G
(BEST1)
|
ENSP00000399709.2:n.*1574A>G
|
|
ENST00000526640.5:c.*4T>C
(FTH1)
|
ENSP00000433321.1:n.*4T>C
|
|
ENST00000529191.5:c.114+2589T>C
(FTH1)
|
ENSP00000431659.1:n.114+2589T>C
|
|
ENST00000529631.5:c.114+2589T>C
(FTH1)
|
ENSP00000431575.1:n.114+2589T>C
|
|
ENST00000530019.5:c.261+646T>C
(FTH1)
|
ENSP00000433470.1:n.261+646T>C
|
|
ENST00000532601.1:c.*4T>C
(FTH1)
|
ENSP00000435111.1:n.*4T>C
|
|
ENST00000532829.5:c.*261T>C
(FTH1)
|
ENSP00000432223.1:n.*261T>C
|
|
ENST00000534180.1:c.*465T>C
(FTH1)
|
ENSP00000434403.1:n.*465T>C
|
|
ENST00000620041.4:c.*4T>C
(FTH1)
|
ENSP00000484477.1:n.*4T>C
|
|
NM_002032.2:c.*4T>C
(FTH1)
|
NP_002023.2:n.*4T>C
|
|
NM_002032.3:c.*4T>C
(FTH1)
MANE Select
|
NP_002023.2:n.*4T>C
|
|
NM_001139443.2:c.*1574A>G
(BEST1)
|
NP_001132915.1:n.*1574A>G
|
|
NM_001363591.2:c.*1574A>G
(BEST1)
|
NP_001350520.1:n.*1574A>G
|
|
NM_001363593.2:c.*1574A>G
(BEST1)
|
NP_001350522.1:n.*1574A>G
|
|