ENST00000248633.9:c.3010T>C
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Tyr1004His
|
|
ENST00000248633.8:c.3010T>C
(PEX1)
|
ENSP00000248633.4:p.Tyr1004His
|
|
ENST00000428214.5:c.2839T>C
(PEX1)
|
ENSP00000394413.1:p.Tyr947His
|
|
ENST00000438045.5:c.2044T>C
(PEX1)
|
ENSP00000410438.1:p.Tyr682His
|
|
ENST00000484913.5:n.3049T>C
(PEX1)
|
|
|
ENST00000496420.5:n.2902T>C
(PEX1)
|
|
|
NM_000466.2:c.3010T>C
(PEX1)
|
NP_000457.1:p.Tyr1004His
|
|
NM_001282677.1:c.2839T>C
(PEX1)
|
NP_001269606.1:p.Tyr947His
|
|
NM_001282678.1:c.2386T>C
(PEX1)
|
NP_001269607.1:p.Tyr796His
|
|
XM_005250433.3:c.1261T>C
(PEX1)
|
XP_005250490.1:p.Tyr421His
|
|
XR_242246.3:n.3106T>C
(PEX1)
|
|
|
XM_017012319.2:c.1261T>C
(PEX1)
|
XP_016867808.1:p.Tyr421His
|
|
XR_001744808.2:n.2037T>C
(PEX1)
|
|
|
XR_001744843.2:n.5282A>G
(GATAD1)
|
|
|
XR_242246.5:n.3057T>C
(PEX1)
|
|
|
XR_927494.3:n.4133A>G
(GATAD1)
|
|
|
XR_927503.3:n.4064A>G
(GATAD1)
|
|
|
NM_000466.3:c.3010T>C
(PEX1)
MANE Select
|
NP_000457.1:p.Tyr1004His
|
|
NM_001282677.2:c.2839T>C
(PEX1)
|
NP_001269606.1:p.Tyr947His
|
|
NM_001282678.2:c.2386T>C
(PEX1)
|
NP_001269607.1:p.Tyr796His
|
|