ENST00000248633.9:c.3683C>A
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Ala1228Asp
|
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ENST00000248633.8:c.3683C>A
(PEX1)
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ENSP00000248633.4:p.Ala1228Asp
|
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ENST00000428214.5:c.3512C>A
(PEX1)
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ENSP00000394413.1:p.Ala1171Asp
|
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ENST00000438045.5:c.2717C>A
(PEX1)
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ENSP00000410438.1:p.Ala906Asp
|
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ENST00000469417.1:n.580C>A
(PEX1)
|
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ENST00000477342.1:n.418C>A
(PEX1)
|
|
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ENST00000484913.5:n.3722C>A
(PEX1)
|
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ENST00000496420.5:n.4733C>A
(PEX1)
|
|
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NM_000466.2:c.3683C>A
(PEX1)
|
NP_000457.1:p.Ala1228Asp
|
|
NM_001282677.1:c.3512C>A
(PEX1)
|
NP_001269606.1:p.Ala1171Asp
|
|
NM_001282678.1:c.3059C>A
(PEX1)
|
NP_001269607.1:p.Ala1020Asp
|
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XM_005250433.3:c.1934C>A
(PEX1)
|
XP_005250490.1:p.Ala645Asp
|
|
XR_242246.3:n.3774C>A
(PEX1)
|
|
|
XR_927494.1:n.1036-1866G>T
(GATAD1)
|
|
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XR_927495.1:n.1036-709G>T
(GATAD1)
|
|
|
XR_927496.1:n.1041-1866G>T
(GATAD1)
|
|
|
XR_927497.1:n.1036-709G>T
(GATAD1)
|
|
|
XR_927498.1:n.1124-1866G>T
(GATAD1)
|
|
|
XR_927500.1:n.1033-1866G>T
(GATAD1)
|
|
|
XR_927502.1:n.1033-709G>T
(GATAD1)
|
|
|
XR_927503.1:n.967-1866G>T
(GATAD1)
|
|
|
XM_017012319.2:c.1934C>A
(PEX1)
|
XP_016867808.1:p.Ala645Asp
|
|
XR_001744808.2:n.2705C>A
(PEX1)
|
|
|
XR_001744842.2:n.2281-1866G>T
(GATAD1)
|
|
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XR_001744843.2:n.2212-1866G>T
(GATAD1)
|
|
|
XR_002956472.1:n.2281-709G>T
(GATAD1)
|
|
|
XR_002956473.1:n.2369-1866G>T
(GATAD1)
|
|
|
XR_002956474.1:n.2286-1866G>T
(GATAD1)
|
|
|
XR_242246.5:n.3725C>A
(PEX1)
|
|
|
XR_927494.3:n.1063-1866G>T
(GATAD1)
|
|
|
XR_927500.3:n.1060-1866G>T
(GATAD1)
|
|
|
XR_927503.3:n.994-1866G>T
(GATAD1)
|
|
|
NM_000466.3:c.3683C>A
(PEX1)
MANE Select
|
NP_000457.1:p.Ala1228Asp
|
|
NM_001282677.2:c.3512C>A
(PEX1)
|
NP_001269606.1:p.Ala1171Asp
|
|
NM_001282678.2:c.3059C>A
(PEX1)
|
NP_001269607.1:p.Ala1020Asp
|
|