ENST00000620041.5:c.423G>C
(FTH1)
|
ENSP00000484477.1:p.Glu141Asp
|
|
ENST00000273550.12:c.423G>C
(FTH1)
MANE Select
|
ENSP00000273550.7:p.Glu141Asp
|
|
ENST00000273550.11:c.423G>C
(FTH1)
|
ENSP00000273550.7:p.Glu141Asp
|
|
ENST00000449131.6:c.*1707C>G
(BEST1)
|
ENSP00000399709.2:n.*1707C>G
|
|
ENST00000526640.5:c.333G>C
(FTH1)
|
ENSP00000433321.1:p.Glu111Asp
|
|
ENST00000529191.5:c.114+2456G>C
(FTH1)
|
ENSP00000431659.1:n.114+2456G>C
|
|
ENST00000529631.5:c.114+2456G>C
(FTH1)
|
ENSP00000431575.1:n.114+2456G>C
|
|
ENST00000530019.5:c.261+513G>C
(FTH1)
|
ENSP00000433470.1:n.261+513G>C
|
|
ENST00000532601.1:c.213G>C
(FTH1)
|
ENSP00000435111.1:p.Glu71Asp
|
|
ENST00000532829.5:c.*128G>C
(FTH1)
|
ENSP00000432223.1:n.*128G>C
|
|
ENST00000533138.1:n.867G>C
(FTH1)
|
|
|
ENST00000534180.1:c.*332G>C
(FTH1)
|
ENSP00000434403.1:n.*332G>C
|
|
ENST00000534719.1:n.679G>C
(FTH1)
|
|
|
ENST00000620041.4:c.423G>C
(FTH1)
|
ENSP00000484477.1:p.Glu141Asp
|
|
NM_002032.2:c.423G>C
(FTH1)
|
NP_002023.2:p.Glu141Asp
|
|
NM_002032.3:c.423G>C
(FTH1)
MANE Select
|
NP_002023.2:p.Glu141Asp
|
|
NM_001139443.2:c.*1707C>G
(BEST1)
|
NP_001132915.1:n.*1707C>G
|
|
NM_001363591.2:c.*1707C>G
(BEST1)
|
NP_001350520.1:n.*1707C>G
|
|
NM_001363593.2:c.*1707C>G
(BEST1)
|
NP_001350522.1:n.*1707C>G
|
|