ENST00000623882.4:c.*798G>T
(CERS1)
MANE Select
|
ENSP00000485308.1:n.*798G>T
|
|
ENST00000247005.8:c.529G>T
(GDF1)
MANE Select
|
ENSP00000247005.5:p.Asp177Tyr
|
|
ENST00000247005.7:c.529G>T
(GDF1)
|
ENSP00000247005.5:p.Asp177Tyr
|
|
ENST00000623882.3:c.*798G>T
(CERS1)
|
ENSP00000485308.1:n.*798G>T
|
|
ENST00000623927.1:c.529G>T
(CERS1)
|
ENSP00000485582.1:p.Asp177Tyr
|
|
NM_001492.5:c.529G>T
(GDF1)
|
NP_001483.3:p.Asp177Tyr
|
|
NM_021267.4:c.*798G>T
(CERS1)
|
NP_067090.1:n.*798G>T
|
|
NM_001492.6:c.529G>T
(GDF1)
MANE Select
|
NP_001483.3:p.Asp177Tyr
|
|
NM_021267.5:c.*798G>T
(CERS1)
MANE Select
|
NP_067090.1:n.*798G>T
|
|
NM_001387438.1:c.529G>T
(GDF1)
|
NP_001374367.1:p.Asp177Tyr
|
|
NM_001387440.1:c.*1390G>T
(CERS1)
|
NP_001374369.1:n.*1390G>T
|
|