ENST00000248633.9:c.3226G>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Asp1076Tyr
|
|
ENST00000248633.8:c.3226G>T
(PEX1)
|
ENSP00000248633.4:p.Asp1076Tyr
|
|
ENST00000428214.5:c.3055G>T
(PEX1)
|
ENSP00000394413.1:p.Asp1019Tyr
|
|
ENST00000438045.5:c.2260G>T
(PEX1)
|
ENSP00000410438.1:p.Asp754Tyr
|
|
ENST00000484913.5:n.3265G>T
(PEX1)
|
|
|
ENST00000496420.5:n.4281G>T
(PEX1)
|
|
|
NM_000466.2:c.3226G>T
(PEX1)
|
NP_000457.1:p.Asp1076Tyr
|
|
NM_001282677.1:c.3055G>T
(PEX1)
|
NP_001269606.1:p.Asp1019Tyr
|
|
NM_001282678.1:c.2602G>T
(PEX1)
|
NP_001269607.1:p.Asp868Tyr
|
|
XM_005250433.3:c.1477G>T
(PEX1)
|
XP_005250490.1:p.Asp493Tyr
|
|
XR_242246.3:n.3322G>T
(PEX1)
|
|
|
XM_017012319.2:c.1477G>T
(PEX1)
|
XP_016867808.1:p.Asp493Tyr
|
|
XR_001744808.2:n.2253G>T
(PEX1)
|
|
|
XR_001744842.2:n.2522C>A
(GATAD1)
|
|
|
XR_001744843.2:n.2453C>A
(GATAD1)
|
|
|
XR_002956472.1:n.2579C>A
(GATAD1)
|
|
|
XR_002956473.1:n.2610C>A
(GATAD1)
|
|
|
XR_002956474.1:n.2527C>A
(GATAD1)
|
|
|
XR_242246.5:n.3273G>T
(PEX1)
|
|
|
XR_927494.3:n.1304C>A
(GATAD1)
|
|
|
XR_927500.3:n.1301C>A
(GATAD1)
|
|
|
XR_927503.3:n.1235C>A
(GATAD1)
|
|
|
NM_000466.3:c.3226G>T
(PEX1)
MANE Select
|
NP_000457.1:p.Asp1076Tyr
|
|
NM_001282677.2:c.3055G>T
(PEX1)
|
NP_001269606.1:p.Asp1019Tyr
|
|
NM_001282678.2:c.2602G>T
(PEX1)
|
NP_001269607.1:p.Asp868Tyr
|
|