ENST00000273550.12:c.*277G>T
(FTH1)
MANE Select
|
ENSP00000273550.7:n.*277G>T
|
|
ENST00000378043.9:c.*328C>A
(BEST1)
MANE Select
|
ENSP00000367282.4:n.*328C>A
|
|
ENST00000273550.11:c.*277G>T
(FTH1)
|
ENSP00000273550.7:n.*277G>T
|
|
ENST00000378043.8:c.*328C>A
(BEST1)
|
ENSP00000367282.4:n.*328C>A
|
|
ENST00000449131.6:c.*1301C>A
(BEST1)
|
ENSP00000399709.2:n.*1301C>A
|
|
ENST00000524926.5:c.*981C>A
(BEST1)
|
ENSP00000432681.1:n.*981C>A
|
|
ENST00000529191.5:c.114+2862G>T
(FTH1)
|
ENSP00000431659.1:n.114+2862G>T
|
|
ENST00000529631.5:c.114+2862G>T
(FTH1)
|
ENSP00000431575.1:n.114+2862G>T
|
|
ENST00000530019.5:c.261+919G>T
(FTH1)
|
ENSP00000433470.1:n.261+919G>T
|
|
NM_001300786.1:c.*328C>A
(BEST1)
|
NP_001287715.1:n.*328C>A
|
|
NM_001300787.1:c.*328C>A
(BEST1)
|
NP_001287716.1:n.*328C>A
|
|
NM_002032.2:c.*277G>T
(FTH1)
|
NP_002023.2:n.*277G>T
|
|
NM_004183.3:c.*328C>A
(BEST1)
|
NP_004174.1:n.*328C>A
|
|
XM_005274210.2:c.*1301C>A
(BEST1)
|
XP_005274267.1:n.*1301C>A
|
|
XM_005274215.2:c.*328C>A
(BEST1)
|
XP_005274272.1:n.*328C>A
|
|
XM_011545229.1:c.*1301C>A
(BEST1)
|
XP_011543531.1:n.*1301C>A
|
|
XM_011545230.1:c.*1301C>A
(BEST1)
|
XP_011543532.1:n.*1301C>A
|
|
XM_011545231.1:c.*1301C>A
(BEST1)
|
XP_011543533.1:n.*1301C>A
|
|
XM_011545233.1:c.*1301C>A
(BEST1)
|
XP_011543535.1:n.*1301C>A
|
|
NM_001363591.1:c.*1301C>A
(BEST1)
|
NP_001350520.1:n.*1301C>A
|
|
NM_001363592.1:c.*2191C>A
(BEST1)
|
NP_001350521.1:n.*2191C>A
|
|
NM_001363593.1:c.*1301C>A
(BEST1)
|
NP_001350522.1:n.*1301C>A
|
|
NR_134580.1:n.2869C>A
(BEST1)
|
|
|
XM_005274210.4:c.*1301C>A
(BEST1)
|
XP_005274267.1:n.*1301C>A
|
|
XM_005274215.4:c.*328C>A
(BEST1)
|
XP_005274272.1:n.*328C>A
|
|
XM_005274216.4:c.*2191C>A
(BEST1)
|
XP_005274273.1:n.*2191C>A
|
|
XM_005274219.4:c.*2097C>A
(BEST1)
|
XP_005274276.1:n.*2097C>A
|
|
XM_005274221.4:c.*2097C>A
(BEST1)
|
XP_005274278.1:n.*2097C>A
|
|
XM_011545229.3:c.*1301C>A
(BEST1)
|
XP_011543531.1:n.*1301C>A
|
|
XM_011545230.3:c.*1301C>A
(BEST1)
|
XP_011543532.1:n.*1301C>A
|
|
XM_011545233.3:c.*1301C>A
(BEST1)
|
XP_011543535.1:n.*1301C>A
|
|
XM_017018230.2:c.*2191C>A
(BEST1)
|
XP_016873719.1:n.*2191C>A
|
|
NM_002032.3:c.*277G>T
(FTH1)
MANE Select
|
NP_002023.2:n.*277G>T
|
|
NM_004183.4:c.*328C>A
(BEST1)
MANE Select
|
NP_004174.1:n.*328C>A
|
|
NM_001139443.2:c.*1301C>A
(BEST1)
|
NP_001132915.1:n.*1301C>A
|
|
NM_001300786.2:c.*328C>A
(BEST1)
|
NP_001287715.1:n.*328C>A
|
|
NM_001300787.2:c.*328C>A
(BEST1)
|
NP_001287716.1:n.*328C>A
|
|
NM_001363591.2:c.*1301C>A
(BEST1)
|
NP_001350520.1:n.*1301C>A
|
|
NM_001363593.2:c.*1301C>A
(BEST1)
|
NP_001350522.1:n.*1301C>A
|
|
NR_134580.2:n.2402C>A
(BEST1)
|
|
|