ENST00000248633.9:c.2930T>G
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Val977Gly
|
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ENST00000248633.8:c.2930T>G
(PEX1)
|
ENSP00000248633.4:p.Val977Gly
|
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ENST00000428214.5:c.2759T>G
(PEX1)
|
ENSP00000394413.1:p.Val920Gly
|
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ENST00000438045.5:c.1964T>G
(PEX1)
|
ENSP00000410438.1:p.Val655Gly
|
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ENST00000484913.5:n.2969T>G
(PEX1)
|
|
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ENST00000496420.5:n.2822T>G
(PEX1)
|
|
|
NM_000466.2:c.2930T>G
(PEX1)
|
NP_000457.1:p.Val977Gly
|
|
NM_001282677.1:c.2759T>G
(PEX1)
|
NP_001269606.1:p.Val920Gly
|
|
NM_001282678.1:c.2306T>G
(PEX1)
|
NP_001269607.1:p.Val769Gly
|
|
XM_005250433.3:c.1181T>G
(PEX1)
|
XP_005250490.1:p.Val394Gly
|
|
XR_242246.3:n.3026T>G
(PEX1)
|
|
|
XM_017012319.2:c.1181T>G
(PEX1)
|
XP_016867808.1:p.Val394Gly
|
|
XR_001744808.2:n.1957T>G
(PEX1)
|
|
|
XR_001744843.2:n.5362A>C
(GATAD1)
|
|
|
XR_242246.5:n.2977T>G
(PEX1)
|
|
|
XR_927494.3:n.4213A>C
(GATAD1)
|
|
|
XR_927503.3:n.4144A>C
(GATAD1)
|
|
|
NM_000466.3:c.2930T>G
(PEX1)
MANE Select
|
NP_000457.1:p.Val977Gly
|
|
NM_001282677.2:c.2759T>G
(PEX1)
|
NP_001269606.1:p.Val920Gly
|
|
NM_001282678.2:c.2306T>G
(PEX1)
|
NP_001269607.1:p.Val769Gly
|
|