|
ENST00000645291.3:c.3281-2229C>G
(CFAP92)
MANE Select
|
ENSP00000496592.2:n.3281-2229C>G
|
|
|
ENST00000308982.12:c.1821G>C
(ACAD9)
MANE Select
|
ENSP00000312618.7:p.Glu607Asp
|
|
|
ENST00000511325.2:n.2498G>C
(ACAD9)
|
|
|
|
ENST00000637488.2:c.861-2229C>G
(CFAP92)
|
|
|
|
ENST00000645291.2:c.3281-2229C>G
(CFAP92)
|
ENSP00000496592.2:n.3281-2229C>G
|
|
|
ENST00000679399.1:c.*1992G>C
(ACAD9)
|
ENSP00000505434.1:n.*1992G>C
|
|
|
ENST00000679431.1:c.*1697G>C
(ACAD9)
|
ENSP00000506440.1:n.*1697G>C
|
|
|
ENST00000679613.1:c.*188G>C
(ACAD9)
|
ENSP00000504971.1:n.*188G>C
|
|
|
ENST00000679715.1:c.1452G>C
(ACAD9)
|
ENSP00000506228.1:p.Glu484Asp
|
|
|
ENST00000679824.1:c.*3127G>C
(ACAD9)
|
ENSP00000505516.1:n.*3127G>C
|
|
|
ENST00000679990.1:n.2655G>C
(ACAD9)
|
|
|
|
ENST00000680636.1:c.*34G>C
(ACAD9)
|
ENSP00000504886.1:n.*34G>C
|
|
|
ENST00000680638.1:n.3866G>C
(ACAD9)
|
|
|
|
ENST00000680744.1:c.*1174G>C
(ACAD9)
|
ENSP00000505243.1:n.*1174G>C
|
|
|
ENST00000680764.1:c.*3225G>C
(ACAD9)
|
ENSP00000505126.1:n.*3225G>C
|
|
|
ENST00000681319.1:n.2607G>C
(ACAD9)
|
|
|
|
ENST00000681367.1:c.*38G>C
(ACAD9)
|
ENSP00000505309.1:n.*38G>C
|
|
|
ENST00000681552.1:c.*38G>C
(ACAD9)
|
ENSP00000505699.1:n.*38G>C
|
|
|
ENST00000681583.1:c.1821G>C
(ACAD9)
|
ENSP00000506340.1:p.Glu607Asp
|
|
|
ENST00000681585.1:c.*440G>C
(ACAD9)
|
ENSP00000506316.1:n.*440G>C
|
|
|
ENST00000681784.1:n.3089G>C
(ACAD9)
|
|
|
|
ENST00000681886.1:c.*1613G>C
(ACAD9)
|
ENSP00000506500.1:n.*1613G>C
|
|
|
ENST00000308982.11:c.1821G>C
(ACAD9)
|
ENSP00000312618.7:p.Glu607Asp
|
|
|
ENST00000505867.5:c.*1621G>C
(ACAD9)
|
ENSP00000425346.1:n.*1621G>C
|
|
|
ENST00000508239.1:c.1685-2229C>G
|
ENSP00000424951.1:n.1685-2229C>G
|
|
|
ENST00000508971.1:c.1110G>C
(ACAD9)
|
ENSP00000422683.1:p.Glu370Asp
|
|
|
ENST00000511227.5:c.*1715G>C
(ACAD9)
|
ENSP00000425226.1:n.*1715G>C
|
|
|
ENST00000511325.1:n.1401G>C
(ACAD9)
|
|
|
|
ENST00000511438.5:c.1169-2229C>G
(CFAP92)
|
ENSP00000426217.1:n.1169-2229C>G
|
|
|
ENST00000511526.5:n.1354G>C
(ACAD9)
|
|
|
|
ENST00000620948.3:c.248G>C
(ACAD9)
|
ENSP00000478191.1:p.Arg83Thr
|
|
|
NM_014049.4:c.1821G>C
(ACAD9)
|
NP_054768.2:p.Glu607Asp
|
|
|
NR_033426.1:n.2199G>C
(ACAD9)
|
|
|
|
XM_011512742.1:c.1452G>C
(ACAD9)
|
XP_011511044.1:p.Glu484Asp
|
|
|
XM_011513047.1:c.3398-2229C>G
(CFAP92)
|
XP_011511349.1:n.3398-2229C>G
|
|
|
XM_011513048.1:c.3267-2229C>G
(CFAP92)
|
XP_011511350.1:n.3267-2229C>G
|
|
|
XM_011513049.1:c.3267-2233C>G
(CFAP92)
|
XP_011511351.1:n.3267-2233C>G
|
|
|
XM_011513050.1:c.3323-2229C>G
(CFAP92)
|
XP_011511352.1:n.3323-2229C>G
|
|
|
NM_001348520.1:c.2408-2229C>G
(CFAP92)
|
NP_001335449.1:n.2408-2229C>G
|
|
|
NM_001348521.1:c.2312-2229C>G
(CFAP92)
|
NP_001335450.1:n.2312-2229C>G
|
|
|
XM_011513050.2:c.3377-2229C>G
(CFAP92)
|
XP_011511352.2:n.3377-2229C>G
|
|
|
XM_017006939.2:c.*2393C>G
(CFAP92)
|
XP_016862428.1:n.*2393C>G
|
|
|
XM_017006940.2:c.*2393C>G
(CFAP92)
|
XP_016862429.1:n.*2393C>G
|
|
|
XM_017006941.2:c.*2393C>G
(CFAP92)
|
XP_016862430.1:n.*2393C>G
|
|
|
XM_017006942.2:c.*2393C>G
(CFAP92)
|
XP_016862431.1:n.*2393C>G
|
|
|
XM_017006944.2:c.*2393C>G
(CFAP92)
|
XP_016862433.1:n.*2393C>G
|
|
|
XM_017006945.1:c.3281-2229C>G
(CFAP92)
|
XP_016862434.1:n.3281-2229C>G
|
|
|
XM_017006946.2:c.*2393C>G
(CFAP92)
|
XP_016862435.1:n.*2393C>G
|
|
|
XM_017006947.2:c.5528C>G
(CFAP92)
|
XP_016862436.1:n.5528C>G
|
|
|
XM_017006948.2:c.*2393C>G
(CFAP92)
|
XP_016862437.1:n.*2393C>G
|
|
|
XM_017006950.2:c.*2393C>G
(CFAP92)
|
XP_016862439.1:n.*2393C>G
|
|
|
XM_017006951.2:c.*2393C>G
(CFAP92)
|
XP_016862440.1:n.*2393C>G
|
|
|
XM_017006952.2:c.*2393C>G
(CFAP92)
|
XP_016862441.1:n.*2393C>G
|
|
|
XM_017006953.2:c.*2393C>G
(CFAP92)
|
XP_016862442.1:n.*2393C>G
|
|
|
XM_017006954.1:c.1919-2229C>G
(CFAP92)
|
XP_016862443.1:n.1919-2229C>G
|
|
|
XM_024453484.1:c.1452G>C
(ACAD9)
|
XP_024309252.1:p.Glu484Asp
|
|
|
XM_024453485.1:c.1452G>C
(ACAD9)
|
XP_024309253.1:p.Glu484Asp
|
|
|
XM_024453688.1:c.*2393C>G
(CFAP92)
|
XP_024309456.1:n.*2393C>G
|
|
|
XM_024453689.1:c.*2393C>G
(CFAP92)
|
XP_024309457.1:n.*2393C>G
|
|
|
XR_427367.3:n.1897G>C
(ACAD9)
|
|
|
|
NM_014049.5:c.1821G>C
(ACAD9)
MANE Select
|
NP_054768.2:p.Glu607Asp
|
|
|
NM_001348520.2:c.2408-2229C>G
(CFAP92)
|
NP_001335449.1:n.2408-2229C>G
|
|
|
NM_001348521.2:c.2312-2229C>G
(CFAP92)
|
NP_001335450.1:n.2312-2229C>G
|
|
|
NM_001394090.1:c.3281-2229C>G
(CFAP92)
MANE Select
|
NP_001381019.1:n.3281-2229C>G
|
|
|
NR_033426.2:n.2069G>C
(ACAD9)
|
|
|
