ENST00000248633.9:c.3025G>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Asp1009Tyr
|
|
ENST00000248633.8:c.3025G>T
(PEX1)
|
ENSP00000248633.4:p.Asp1009Tyr
|
|
ENST00000428214.5:c.2854G>T
(PEX1)
|
ENSP00000394413.1:p.Asp952Tyr
|
|
ENST00000438045.5:c.2059G>T
(PEX1)
|
ENSP00000410438.1:p.Asp687Tyr
|
|
ENST00000484913.5:n.3064G>T
(PEX1)
|
|
|
ENST00000496420.5:n.2917G>T
(PEX1)
|
|
|
NM_000466.2:c.3025G>T
(PEX1)
|
NP_000457.1:p.Asp1009Tyr
|
|
NM_001282677.1:c.2854G>T
(PEX1)
|
NP_001269606.1:p.Asp952Tyr
|
|
NM_001282678.1:c.2401G>T
(PEX1)
|
NP_001269607.1:p.Asp801Tyr
|
|
XM_005250433.3:c.1276G>T
(PEX1)
|
XP_005250490.1:p.Asp426Tyr
|
|
XR_242246.3:n.3121G>T
(PEX1)
|
|
|
XM_017012319.2:c.1276G>T
(PEX1)
|
XP_016867808.1:p.Asp426Tyr
|
|
XR_001744808.2:n.2052G>T
(PEX1)
|
|
|
XR_001744843.2:n.5267C>A
(GATAD1)
|
|
|
XR_242246.5:n.3072G>T
(PEX1)
|
|
|
XR_927494.3:n.4118C>A
(GATAD1)
|
|
|
XR_927503.3:n.4049C>A
(GATAD1)
|
|
|
NM_000466.3:c.3025G>T
(PEX1)
MANE Select
|
NP_000457.1:p.Asp1009Tyr
|
|
NM_001282677.2:c.2854G>T
(PEX1)
|
NP_001269606.1:p.Asp952Tyr
|
|
NM_001282678.2:c.2401G>T
(PEX1)
|
NP_001269607.1:p.Asp801Tyr
|
|