ENST00000273550.12:c.*190A>G
(FTH1)
MANE Select
|
ENSP00000273550.7:n.*190A>G
|
|
ENST00000273550.11:c.*190A>G
(FTH1)
|
ENSP00000273550.7:n.*190A>G
|
|
ENST00000449131.6:c.*1388T>C
(BEST1)
|
ENSP00000399709.2:n.*1388T>C
|
|
ENST00000529191.5:c.114+2775A>G
(FTH1)
|
ENSP00000431659.1:n.114+2775A>G
|
|
ENST00000529631.5:c.114+2775A>G
(FTH1)
|
ENSP00000431575.1:n.114+2775A>G
|
|
ENST00000530019.5:c.261+832A>G
(FTH1)
|
ENSP00000433470.1:n.261+832A>G
|
|
NM_002032.2:c.*190A>G
(FTH1)
|
NP_002023.2:n.*190A>G
|
|
NM_002032.3:c.*190A>G
(FTH1)
MANE Select
|
NP_002023.2:n.*190A>G
|
|
NM_001139443.2:c.*1388T>C
(BEST1)
|
NP_001132915.1:n.*1388T>C
|
|
NM_001363591.2:c.*1388T>C
(BEST1)
|
NP_001350520.1:n.*1388T>C
|
|
NM_001363593.2:c.*1388T>C
(BEST1)
|
NP_001350522.1:n.*1388T>C
|
|