ENST00000273550.12:c.*181T>G
(FTH1)
MANE Select
|
ENSP00000273550.7:n.*181T>G
|
|
ENST00000273550.11:c.*181T>G
(FTH1)
|
ENSP00000273550.7:n.*181T>G
|
|
ENST00000449131.6:c.*1397A>C
(BEST1)
|
ENSP00000399709.2:n.*1397A>C
|
|
ENST00000529191.5:c.114+2766T>G
(FTH1)
|
ENSP00000431659.1:n.114+2766T>G
|
|
ENST00000529631.5:c.114+2766T>G
(FTH1)
|
ENSP00000431575.1:n.114+2766T>G
|
|
ENST00000530019.5:c.261+823T>G
(FTH1)
|
ENSP00000433470.1:n.261+823T>G
|
|
NM_002032.2:c.*181T>G
(FTH1)
|
NP_002023.2:n.*181T>G
|
|
NM_002032.3:c.*181T>G
(FTH1)
MANE Select
|
NP_002023.2:n.*181T>G
|
|
NM_001139443.2:c.*1397A>C
(BEST1)
|
NP_001132915.1:n.*1397A>C
|
|
NM_001363591.2:c.*1397A>C
(BEST1)
|
NP_001350520.1:n.*1397A>C
|
|
NM_001363593.2:c.*1397A>C
(BEST1)
|
NP_001350522.1:n.*1397A>C
|
|