ENST00000248633.9:c.3005G>A
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Cys1002Tyr
|
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ENST00000248633.8:c.3005G>A
(PEX1)
|
ENSP00000248633.4:p.Cys1002Tyr
|
|
ENST00000428214.5:c.2834G>A
(PEX1)
|
ENSP00000394413.1:p.Cys945Tyr
|
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ENST00000438045.5:c.2039G>A
(PEX1)
|
ENSP00000410438.1:p.Cys680Tyr
|
|
ENST00000484913.5:n.3044G>A
(PEX1)
|
|
|
ENST00000496420.5:n.2897G>A
(PEX1)
|
|
|
NM_000466.2:c.3005G>A
(PEX1)
|
NP_000457.1:p.Cys1002Tyr
|
|
NM_001282677.1:c.2834G>A
(PEX1)
|
NP_001269606.1:p.Cys945Tyr
|
|
NM_001282678.1:c.2381G>A
(PEX1)
|
NP_001269607.1:p.Cys794Tyr
|
|
XM_005250433.3:c.1256G>A
(PEX1)
|
XP_005250490.1:p.Cys419Tyr
|
|
XR_242246.3:n.3101G>A
(PEX1)
|
|
|
XM_017012319.2:c.1256G>A
(PEX1)
|
XP_016867808.1:p.Cys419Tyr
|
|
XR_001744808.2:n.2032G>A
(PEX1)
|
|
|
XR_001744843.2:n.5287C>T
(GATAD1)
|
|
|
XR_242246.5:n.3052G>A
(PEX1)
|
|
|
XR_927494.3:n.4138C>T
(GATAD1)
|
|
|
XR_927503.3:n.4069C>T
(GATAD1)
|
|
|
NM_000466.3:c.3005G>A
(PEX1)
MANE Select
|
NP_000457.1:p.Cys1002Tyr
|
|
NM_001282677.2:c.2834G>A
(PEX1)
|
NP_001269606.1:p.Cys945Tyr
|
|
NM_001282678.2:c.2381G>A
(PEX1)
|
NP_001269607.1:p.Cys794Tyr
|
|