ENST00000248633.9:c.2996T>G
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Leu999Arg
|
|
ENST00000248633.8:c.2996T>G
(PEX1)
|
ENSP00000248633.4:p.Leu999Arg
|
|
ENST00000428214.5:c.2825T>G
(PEX1)
|
ENSP00000394413.1:p.Leu942Arg
|
|
ENST00000438045.5:c.2030T>G
(PEX1)
|
ENSP00000410438.1:p.Leu677Arg
|
|
ENST00000484913.5:n.3035T>G
(PEX1)
|
|
|
ENST00000496420.5:n.2888T>G
(PEX1)
|
|
|
NM_000466.2:c.2996T>G
(PEX1)
|
NP_000457.1:p.Leu999Arg
|
|
NM_001282677.1:c.2825T>G
(PEX1)
|
NP_001269606.1:p.Leu942Arg
|
|
NM_001282678.1:c.2372T>G
(PEX1)
|
NP_001269607.1:p.Leu791Arg
|
|
XM_005250433.3:c.1247T>G
(PEX1)
|
XP_005250490.1:p.Leu416Arg
|
|
XR_242246.3:n.3092T>G
(PEX1)
|
|
|
XM_017012319.2:c.1247T>G
(PEX1)
|
XP_016867808.1:p.Leu416Arg
|
|
XR_001744808.2:n.2023T>G
(PEX1)
|
|
|
XR_001744843.2:n.5296A>C
(GATAD1)
|
|
|
XR_242246.5:n.3043T>G
(PEX1)
|
|
|
XR_927494.3:n.4147A>C
(GATAD1)
|
|
|
XR_927503.3:n.4078A>C
(GATAD1)
|
|
|
NM_000466.3:c.2996T>G
(PEX1)
MANE Select
|
NP_000457.1:p.Leu999Arg
|
|
NM_001282677.2:c.2825T>G
(PEX1)
|
NP_001269606.1:p.Leu942Arg
|
|
NM_001282678.2:c.2372T>G
(PEX1)
|
NP_001269607.1:p.Leu791Arg
|
|