ENST00000248633.9:c.2991T>C
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Gly997=
|
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ENST00000248633.8:c.2991T>C
(PEX1)
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ENSP00000248633.4:p.Gly997=
|
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ENST00000428214.5:c.2820T>C
(PEX1)
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ENSP00000394413.1:p.Gly940=
|
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ENST00000438045.5:c.2025T>C
(PEX1)
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ENSP00000410438.1:p.Gly675=
|
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ENST00000484913.5:n.3030T>C
(PEX1)
|
|
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ENST00000496420.5:n.2883T>C
(PEX1)
|
|
|
NM_000466.2:c.2991T>C
(PEX1)
|
NP_000457.1:p.Gly997=
|
|
NM_001282677.1:c.2820T>C
(PEX1)
|
NP_001269606.1:p.Gly940=
|
|
NM_001282678.1:c.2367T>C
(PEX1)
|
NP_001269607.1:p.Gly789=
|
|
XM_005250433.3:c.1242T>C
(PEX1)
|
XP_005250490.1:p.Gly414=
|
|
XR_242246.3:n.3087T>C
(PEX1)
|
|
|
XM_017012319.2:c.1242T>C
(PEX1)
|
XP_016867808.1:p.Gly414=
|
|
XR_001744808.2:n.2018T>C
(PEX1)
|
|
|
XR_001744843.2:n.5301A>G
(GATAD1)
|
|
|
XR_242246.5:n.3038T>C
(PEX1)
|
|
|
XR_927494.3:n.4152A>G
(GATAD1)
|
|
|
XR_927503.3:n.4083A>G
(GATAD1)
|
|
|
NM_000466.3:c.2991T>C
(PEX1)
MANE Select
|
NP_000457.1:p.Gly997=
|
|
NM_001282677.2:c.2820T>C
(PEX1)
|
NP_001269606.1:p.Gly940=
|
|
NM_001282678.2:c.2367T>C
(PEX1)
|
NP_001269607.1:p.Gly789=
|
|