ENST00000248633.9:c.3235C>G
(PEX1)
MANE Select
|
ENSP00000248633.4:p.Leu1079Val
|
|
ENST00000248633.8:c.3235C>G
(PEX1)
|
ENSP00000248633.4:p.Leu1079Val
|
|
ENST00000428214.5:c.3064C>G
(PEX1)
|
ENSP00000394413.1:p.Leu1022Val
|
|
ENST00000438045.5:c.2269C>G
(PEX1)
|
ENSP00000410438.1:p.Leu757Val
|
|
ENST00000484913.5:n.3274C>G
(PEX1)
|
|
|
ENST00000496420.5:n.4290C>G
(PEX1)
|
|
|
NM_000466.2:c.3235C>G
(PEX1)
|
NP_000457.1:p.Leu1079Val
|
|
NM_001282677.1:c.3064C>G
(PEX1)
|
NP_001269606.1:p.Leu1022Val
|
|
NM_001282678.1:c.2611C>G
(PEX1)
|
NP_001269607.1:p.Leu871Val
|
|
XM_005250433.3:c.1486C>G
(PEX1)
|
XP_005250490.1:p.Leu496Val
|
|
XR_242246.3:n.3331C>G
(PEX1)
|
|
|
XM_017012319.2:c.1486C>G
(PEX1)
|
XP_016867808.1:p.Leu496Val
|
|
XR_001744808.2:n.2262C>G
(PEX1)
|
|
|
XR_001744842.2:n.2513G>C
(GATAD1)
|
|
|
XR_001744843.2:n.2444G>C
(GATAD1)
|
|
|
XR_002956472.1:n.2570G>C
(GATAD1)
|
|
|
XR_002956473.1:n.2601G>C
(GATAD1)
|
|
|
XR_002956474.1:n.2518G>C
(GATAD1)
|
|
|
XR_242246.5:n.3282C>G
(PEX1)
|
|
|
XR_927494.3:n.1295G>C
(GATAD1)
|
|
|
XR_927500.3:n.1292G>C
(GATAD1)
|
|
|
XR_927503.3:n.1226G>C
(GATAD1)
|
|
|
NM_000466.3:c.3235C>G
(PEX1)
MANE Select
|
NP_000457.1:p.Leu1079Val
|
|
NM_001282677.2:c.3064C>G
(PEX1)
|
NP_001269606.1:p.Leu1022Val
|
|
NM_001282678.2:c.2611C>G
(PEX1)
|
NP_001269607.1:p.Leu871Val
|
|