ENST00000248633.9:c.2990G>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Gly997Val
|
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ENST00000248633.8:c.2990G>T
(PEX1)
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ENSP00000248633.4:p.Gly997Val
|
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ENST00000428214.5:c.2819G>T
(PEX1)
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ENSP00000394413.1:p.Gly940Val
|
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ENST00000438045.5:c.2024G>T
(PEX1)
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ENSP00000410438.1:p.Gly675Val
|
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ENST00000484913.5:n.3029G>T
(PEX1)
|
|
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ENST00000496420.5:n.2882G>T
(PEX1)
|
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NM_000466.2:c.2990G>T
(PEX1)
|
NP_000457.1:p.Gly997Val
|
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NM_001282677.1:c.2819G>T
(PEX1)
|
NP_001269606.1:p.Gly940Val
|
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NM_001282678.1:c.2366G>T
(PEX1)
|
NP_001269607.1:p.Gly789Val
|
|
XM_005250433.3:c.1241G>T
(PEX1)
|
XP_005250490.1:p.Gly414Val
|
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XR_242246.3:n.3086G>T
(PEX1)
|
|
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XM_017012319.2:c.1241G>T
(PEX1)
|
XP_016867808.1:p.Gly414Val
|
|
XR_001744808.2:n.2017G>T
(PEX1)
|
|
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XR_001744843.2:n.5302C>A
(GATAD1)
|
|
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XR_242246.5:n.3037G>T
(PEX1)
|
|
|
XR_927494.3:n.4153C>A
(GATAD1)
|
|
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XR_927503.3:n.4084C>A
(GATAD1)
|
|
|
NM_000466.3:c.2990G>T
(PEX1)
MANE Select
|
NP_000457.1:p.Gly997Val
|
|
NM_001282677.2:c.2819G>T
(PEX1)
|
NP_001269606.1:p.Gly940Val
|
|
NM_001282678.2:c.2366G>T
(PEX1)
|
NP_001269607.1:p.Gly789Val
|
|