ENST00000248633.9:c.2966T=
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Ile989=
|
|
ENST00000248633.8:c.2966T=
(PEX1)
|
ENSP00000248633.4:p.Ile989=
|
|
ENST00000428214.5:c.2795T=
(PEX1)
|
ENSP00000394413.1:p.Ile932=
|
|
ENST00000438045.5:c.2000T=
(PEX1)
|
ENSP00000410438.1:p.Ile667=
|
|
ENST00000484913.5:n.3005T=
(PEX1)
|
|
|
ENST00000496420.5:n.2858T=
(PEX1)
|
|
|
NM_000466.2:c.2966T=
(PEX1)
|
NP_000457.1:p.Ile989=
|
|
NM_001282677.1:c.2795T=
(PEX1)
|
NP_001269606.1:p.Ile932=
|
|
NM_001282678.1:c.2342T=
(PEX1)
|
NP_001269607.1:p.Ile781=
|
|
XM_005250433.3:c.1217T=
(PEX1)
|
XP_005250490.1:p.Ile406=
|
|
XR_242246.3:n.3062T=
(PEX1)
|
|
|
XM_017012319.2:c.1217T=
(PEX1)
|
XP_016867808.1:p.Ile406=
|
|
XR_001744808.2:n.1993T=
(PEX1)
|
|
|
XR_001744843.2:n.5326A=
(GATAD1)
|
|
|
XR_242246.5:n.3013T=
(PEX1)
|
|
|
XR_927494.3:n.4177A=
(GATAD1)
|
|
|
XR_927503.3:n.4108A=
(GATAD1)
|
|
|
NM_000466.3:c.2966T=
(PEX1)
MANE Select
|
NP_000457.1:p.Ile989=
|
|
NM_001282677.2:c.2795T=
(PEX1)
|
NP_001269606.1:p.Ile932=
|
|
NM_001282678.2:c.2342T=
(PEX1)
|
NP_001269607.1:p.Ile781=
|
|