ENST00000645291.3:c.*240G=
(CFAP92)
MANE Select
|
ENSP00000496592.2:n.*240G=
|
|
ENST00000308982.12:c.1602C=
(ACAD9)
MANE Select
|
ENSP00000312618.7:p.Ala534=
|
|
ENST00000511325.2:n.2279C=
(ACAD9)
|
|
|
ENST00000645291.2:c.*240G=
(CFAP92)
|
ENSP00000496592.2:n.*240G=
|
|
ENST00000679399.1:c.*1773C=
(ACAD9)
|
ENSP00000505434.1:n.*1773C=
|
|
ENST00000679431.1:c.*1478C=
(ACAD9)
|
ENSP00000506440.1:n.*1478C=
|
|
ENST00000679613.1:c.1602C=
(ACAD9)
|
ENSP00000504971.1:p.Ala534=
|
|
ENST00000679715.1:c.1233C=
(ACAD9)
|
ENSP00000506228.1:p.Ala411=
|
|
ENST00000679824.1:c.*2908C=
(ACAD9)
|
ENSP00000505516.1:n.*2908C=
|
|
ENST00000679990.1:n.2436C=
(ACAD9)
|
|
|
ENST00000680636.1:c.1696C=
(ACAD9)
|
ENSP00000504886.1:p.Gln566=
|
|
ENST00000680638.1:n.1954C=
(ACAD9)
|
|
|
ENST00000680744.1:c.*955C=
(ACAD9)
|
ENSP00000505243.1:n.*955C=
|
|
ENST00000680764.1:c.*3006C=
(ACAD9)
|
ENSP00000505126.1:n.*3006C=
|
|
ENST00000681319.1:n.2388C=
(ACAD9)
|
|
|
ENST00000681367.1:c.1602C=
(ACAD9)
|
ENSP00000505309.1:p.Ala534=
|
|
ENST00000681552.1:c.1150-2448C=
(ACAD9)
|
ENSP00000505699.1:n.1150-2448C=
|
|
ENST00000681583.1:c.1602C=
(ACAD9)
|
ENSP00000506340.1:p.Ala534=
|
|
ENST00000681585.1:c.*221C=
(ACAD9)
|
ENSP00000506316.1:n.*221C=
|
|
ENST00000681784.1:n.2279C=
(ACAD9)
|
|
|
ENST00000681886.1:c.*1394C=
(ACAD9)
|
ENSP00000506500.1:n.*1394C=
|
|
ENST00000308982.11:c.1602C=
(ACAD9)
|
ENSP00000312618.7:p.Ala534=
|
|
ENST00000505867.5:c.*1402C=
(ACAD9)
|
ENSP00000425346.1:n.*1402C=
|
|
ENST00000508239.1:c.*240G=
|
ENSP00000424951.1:n.*240G=
|
|
ENST00000508971.1:c.891C=
(ACAD9)
|
ENSP00000422683.1:p.Ala297=
|
|
ENST00000511227.5:c.*1496C=
(ACAD9)
|
ENSP00000425226.1:n.*1496C=
|
|
ENST00000511325.1:n.1182C=
(ACAD9)
|
|
|
ENST00000511438.5:c.*240G=
(CFAP92)
|
ENSP00000426217.1:n.*240G=
|
|
ENST00000511526.5:n.1135C=
(ACAD9)
|
|
|
ENST00000620948.3:c.31C=
(ACAD9)
|
ENSP00000478191.1:p.Gln11=
|
|
NM_014049.4:c.1602C=
(ACAD9)
|
NP_054768.2:p.Ala534=
|
|
NR_033426.1:n.1980C=
(ACAD9)
|
|
|
XM_011512742.1:c.1233C=
(ACAD9)
|
XP_011511044.1:p.Ala411=
|
|
NM_001348520.1:c.*240G=
(CFAP92)
|
NP_001335449.1:n.*240G=
|
|
NM_001348521.1:c.*240G=
(CFAP92)
|
NP_001335450.1:n.*240G=
|
|
XM_024453484.1:c.1233C=
(ACAD9)
|
XP_024309252.1:p.Ala411=
|
|
XM_024453485.1:c.1233C=
(ACAD9)
|
XP_024309253.1:p.Ala411=
|
|
XR_427367.3:n.1678C=
(ACAD9)
|
|
|
NM_014049.5:c.1602C=
(ACAD9)
MANE Select
|
NP_054768.2:p.Ala534=
|
|
NM_001348520.2:c.*240G=
(CFAP92)
|
NP_001335449.1:n.*240G=
|
|
NM_001348521.2:c.*240G=
(CFAP92)
|
NP_001335450.1:n.*240G=
|
|
NM_001394090.1:c.*240G=
(CFAP92)
MANE Select
|
NP_001381019.1:n.*240G=
|
|
NR_033426.2:n.1850C=
(ACAD9)
|
|
|