ENST00000248633.9:c.2968G>T
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Asp990Tyr
|
|
ENST00000248633.8:c.2968G>T
(PEX1)
|
ENSP00000248633.4:p.Asp990Tyr
|
|
ENST00000428214.5:c.2797G>T
(PEX1)
|
ENSP00000394413.1:p.Asp933Tyr
|
|
ENST00000438045.5:c.2002G>T
(PEX1)
|
ENSP00000410438.1:p.Asp668Tyr
|
|
ENST00000484913.5:n.3007G>T
(PEX1)
|
|
|
ENST00000496420.5:n.2860G>T
(PEX1)
|
|
|
NM_000466.2:c.2968G>T
(PEX1)
|
NP_000457.1:p.Asp990Tyr
|
|
NM_001282677.1:c.2797G>T
(PEX1)
|
NP_001269606.1:p.Asp933Tyr
|
|
NM_001282678.1:c.2344G>T
(PEX1)
|
NP_001269607.1:p.Asp782Tyr
|
|
XM_005250433.3:c.1219G>T
(PEX1)
|
XP_005250490.1:p.Asp407Tyr
|
|
XR_242246.3:n.3064G>T
(PEX1)
|
|
|
XM_017012319.2:c.1219G>T
(PEX1)
|
XP_016867808.1:p.Asp407Tyr
|
|
XR_001744808.2:n.1995G>T
(PEX1)
|
|
|
XR_001744843.2:n.5324C>A
(GATAD1)
|
|
|
XR_242246.5:n.3015G>T
(PEX1)
|
|
|
XR_927494.3:n.4175C>A
(GATAD1)
|
|
|
XR_927503.3:n.4106C>A
(GATAD1)
|
|
|
NM_000466.3:c.2968G>T
(PEX1)
MANE Select
|
NP_000457.1:p.Asp990Tyr
|
|
NM_001282677.2:c.2797G>T
(PEX1)
|
NP_001269606.1:p.Asp933Tyr
|
|
NM_001282678.2:c.2344G>T
(PEX1)
|
NP_001269607.1:p.Asp782Tyr
|
|