|
ENST00000248633.9:c.3627C>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Ser1209=
|
|
|
ENST00000248633.8:c.3627C>T
(PEX1)
|
ENSP00000248633.4:p.Ser1209=
|
|
|
ENST00000428214.5:c.3456C>T
(PEX1)
|
ENSP00000394413.1:p.Ser1152=
|
|
|
ENST00000438045.5:c.2661C>T
(PEX1)
|
ENSP00000410438.1:p.Ser887=
|
|
|
ENST00000469417.1:n.524C>T
(PEX1)
|
|
|
|
ENST00000477342.1:n.72C>T
(PEX1)
|
|
|
|
ENST00000484913.5:n.3666C>T
(PEX1)
|
|
|
|
ENST00000496420.5:n.4682C>T
(PEX1)
|
|
|
|
NM_000466.2:c.3627C>T
(PEX1)
|
NP_000457.1:p.Ser1209=
|
|
|
NM_001282677.1:c.3456C>T
(PEX1)
|
NP_001269606.1:p.Ser1152=
|
|
|
NM_001282678.1:c.3003C>T
(PEX1)
|
NP_001269607.1:p.Ser1001=
|
|
|
XM_005250433.3:c.1878C>T
(PEX1)
|
XP_005250490.1:p.Ser626=
|
|
|
XR_242246.3:n.3723C>T
(PEX1)
|
|
|
|
XR_927494.1:n.1036-1520G>A
(GATAD1)
|
|
|
|
XR_927495.1:n.1036-363G>A
(GATAD1)
|
|
|
|
XR_927496.1:n.1041-1520G>A
(GATAD1)
|
|
|
|
XR_927497.1:n.1036-363G>A
(GATAD1)
|
|
|
|
XR_927498.1:n.1124-1520G>A
(GATAD1)
|
|
|
|
XR_927500.1:n.1033-1520G>A
(GATAD1)
|
|
|
|
XR_927502.1:n.1033-363G>A
(GATAD1)
|
|
|
|
XR_927503.1:n.967-1520G>A
(GATAD1)
|
|
|
|
XM_017012319.2:c.1878C>T
(PEX1)
|
XP_016867808.1:p.Ser626=
|
|
|
XR_001744808.2:n.2654C>T
(PEX1)
|
|
|
|
XR_001744842.2:n.2281-1520G>A
(GATAD1)
|
|
|
|
XR_001744843.2:n.2212-1520G>A
(GATAD1)
|
|
|
|
XR_002956472.1:n.2281-363G>A
(GATAD1)
|
|
|
|
XR_002956473.1:n.2369-1520G>A
(GATAD1)
|
|
|
|
XR_002956474.1:n.2286-1520G>A
(GATAD1)
|
|
|
|
XR_242246.5:n.3674C>T
(PEX1)
|
|
|
|
XR_927494.3:n.1063-1520G>A
(GATAD1)
|
|
|
|
XR_927500.3:n.1060-1520G>A
(GATAD1)
|
|
|
|
XR_927503.3:n.994-1520G>A
(GATAD1)
|
|
|
|
NM_000466.3:c.3627C>T
(PEX1)
MANE Select
|
NP_000457.1:p.Ser1209=
|
|
|
NM_001282677.2:c.3456C>T
(PEX1)
|
NP_001269606.1:p.Ser1152=
|
|
|
NM_001282678.2:c.3003C>T
(PEX1)
|
NP_001269607.1:p.Ser1001=
|
|
