ENST00000248633.9:c.3013T>G
(PEX1)
MANE Select
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ENSP00000248633.4:p.Cys1005Gly
|
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ENST00000248633.8:c.3013T>G
(PEX1)
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ENSP00000248633.4:p.Cys1005Gly
|
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ENST00000428214.5:c.2842T>G
(PEX1)
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ENSP00000394413.1:p.Cys948Gly
|
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ENST00000438045.5:c.2047T>G
(PEX1)
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ENSP00000410438.1:p.Cys683Gly
|
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ENST00000484913.5:n.3052T>G
(PEX1)
|
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ENST00000496420.5:n.2905T>G
(PEX1)
|
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NM_000466.2:c.3013T>G
(PEX1)
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NP_000457.1:p.Cys1005Gly
|
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NM_001282677.1:c.2842T>G
(PEX1)
|
NP_001269606.1:p.Cys948Gly
|
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NM_001282678.1:c.2389T>G
(PEX1)
|
NP_001269607.1:p.Cys797Gly
|
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XM_005250433.3:c.1264T>G
(PEX1)
|
XP_005250490.1:p.Cys422Gly
|
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XR_242246.3:n.3109T>G
(PEX1)
|
|
|
XM_017012319.2:c.1264T>G
(PEX1)
|
XP_016867808.1:p.Cys422Gly
|
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XR_001744808.2:n.2040T>G
(PEX1)
|
|
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XR_001744843.2:n.5279A>C
(GATAD1)
|
|
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XR_242246.5:n.3060T>G
(PEX1)
|
|
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XR_927494.3:n.4130A>C
(GATAD1)
|
|
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XR_927503.3:n.4061A>C
(GATAD1)
|
|
|
NM_000466.3:c.3013T>G
(PEX1)
MANE Select
|
NP_000457.1:p.Cys1005Gly
|
|
NM_001282677.2:c.2842T>G
(PEX1)
|
NP_001269606.1:p.Cys948Gly
|
|
NM_001282678.2:c.2389T>G
(PEX1)
|
NP_001269607.1:p.Cys797Gly
|
|