ENST00000248633.9:c.3232G>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Asp1078Tyr
|
|
ENST00000248633.8:c.3232G>T
(PEX1)
|
ENSP00000248633.4:p.Asp1078Tyr
|
|
ENST00000428214.5:c.3061G>T
(PEX1)
|
ENSP00000394413.1:p.Asp1021Tyr
|
|
ENST00000438045.5:c.2266G>T
(PEX1)
|
ENSP00000410438.1:p.Asp756Tyr
|
|
ENST00000484913.5:n.3271G>T
(PEX1)
|
|
|
ENST00000496420.5:n.4287G>T
(PEX1)
|
|
|
NM_000466.2:c.3232G>T
(PEX1)
|
NP_000457.1:p.Asp1078Tyr
|
|
NM_001282677.1:c.3061G>T
(PEX1)
|
NP_001269606.1:p.Asp1021Tyr
|
|
NM_001282678.1:c.2608G>T
(PEX1)
|
NP_001269607.1:p.Asp870Tyr
|
|
XM_005250433.3:c.1483G>T
(PEX1)
|
XP_005250490.1:p.Asp495Tyr
|
|
XR_242246.3:n.3328G>T
(PEX1)
|
|
|
XM_017012319.2:c.1483G>T
(PEX1)
|
XP_016867808.1:p.Asp495Tyr
|
|
XR_001744808.2:n.2259G>T
(PEX1)
|
|
|
XR_001744842.2:n.2516C>A
(GATAD1)
|
|
|
XR_001744843.2:n.2447C>A
(GATAD1)
|
|
|
XR_002956472.1:n.2573C>A
(GATAD1)
|
|
|
XR_002956473.1:n.2604C>A
(GATAD1)
|
|
|
XR_002956474.1:n.2521C>A
(GATAD1)
|
|
|
XR_242246.5:n.3279G>T
(PEX1)
|
|
|
XR_927494.3:n.1298C>A
(GATAD1)
|
|
|
XR_927500.3:n.1295C>A
(GATAD1)
|
|
|
XR_927503.3:n.1229C>A
(GATAD1)
|
|
|
NM_000466.3:c.3232G>T
(PEX1)
MANE Select
|
NP_000457.1:p.Asp1078Tyr
|
|
NM_001282677.2:c.3061G>T
(PEX1)
|
NP_001269606.1:p.Asp1021Tyr
|
|
NM_001282678.2:c.2608G>T
(PEX1)
|
NP_001269607.1:p.Asp870Tyr
|
|