ENST00000623882.4:c.805C>T
(CERS1)
MANE Select
|
ENSP00000485308.1:p.His269Tyr
|
|
ENST00000247005.8:c.-518C>T
(GDF1)
MANE Select
|
ENSP00000247005.5:n.-518C>T
|
|
ENST00000247005.7:c.-518C>T
(GDF1)
|
ENSP00000247005.5:n.-518C>T
|
|
ENST00000429504.6:c.805C>T
(CERS1)
|
ENSP00000389044.1:p.His269Tyr
|
|
ENST00000542296.6:c.511C>T
(CERS1)
|
ENSP00000437648.1:p.His171Tyr
|
|
ENST00000596048.1:c.362C>T
(CERS1)
|
|
|
ENST00000623882.3:c.805C>T
(CERS1)
|
ENSP00000485308.1:p.His269Tyr
|
|
ENST00000623927.1:c.-518C>T
(CERS1)
|
ENSP00000485582.1:n.-518C>T
|
|
NM_001290265.1:c.511C>T
(CERS1)
|
NP_001277194.1:p.His171Tyr
|
|
NM_001492.5:c.-518C>T
(GDF1)
|
NP_001483.3:n.-518C>T
|
|
NM_021267.4:c.805C>T
(CERS1)
|
NP_067090.1:p.His269Tyr
|
|
NM_198207.2:c.805C>T
(CERS1)
|
NP_937850.1:p.His269Tyr
|
|
NM_001492.6:c.-518C>T
(GDF1)
MANE Select
|
NP_001483.3:n.-518C>T
|
|
NM_021267.5:c.805C>T
(CERS1)
MANE Select
|
NP_067090.1:p.His269Tyr
|
|
NM_198207.3:c.805C>T
(CERS1)
|
NP_937850.1:p.His269Tyr
|
|
NM_001290265.2:c.511C>T
(CERS1)
|
NP_001277194.1:p.His171Tyr
|
|
NM_001387438.1:c.-313+4751C>T
(GDF1)
|
NP_001374367.1:n.-313+4751C>T
|
|
NM_001387439.1:c.805C>T
(CERS1)
|
NP_001374368.1:p.His269Tyr
|
|
NM_001387440.1:c.805C>T
(CERS1)
|
NP_001374369.1:p.His269Tyr
|
|
NM_001387441.1:c.760C>T
(CERS1)
|
NP_001374370.1:p.His254Tyr
|
|
NM_001387442.1:c.511C>T
(CERS1)
|
NP_001374371.1:p.His171Tyr
|
|
NM_001387443.1:c.511C>T
(CERS1)
|
NP_001374372.1:p.His171Tyr
|
|
NM_001387444.1:c.511C>T
(CERS1)
|
NP_001374373.1:p.His171Tyr
|
|
NM_001387445.1:c.511C>T
(CERS1)
|
NP_001374374.1:p.His171Tyr
|
|