ENST00000623882.4:c.*773G>C
(CERS1)
MANE Select
|
ENSP00000485308.1:n.*773G>C
|
|
ENST00000247005.8:c.504G>C
(GDF1)
MANE Select
|
ENSP00000247005.5:p.Ala168=
|
|
ENST00000247005.7:c.504G>C
(GDF1)
|
ENSP00000247005.5:p.Ala168=
|
|
ENST00000623882.3:c.*773G>C
(CERS1)
|
ENSP00000485308.1:n.*773G>C
|
|
ENST00000623927.1:c.504G>C
(CERS1)
|
ENSP00000485582.1:p.Ala168=
|
|
NM_001492.5:c.504G>C
(GDF1)
|
NP_001483.3:p.Ala168=
|
|
NM_021267.4:c.*773G>C
(CERS1)
|
NP_067090.1:n.*773G>C
|
|
NM_001492.6:c.504G>C
(GDF1)
MANE Select
|
NP_001483.3:p.Ala168=
|
|
NM_021267.5:c.*773G>C
(CERS1)
MANE Select
|
NP_067090.1:n.*773G>C
|
|
NM_001387438.1:c.504G>C
(GDF1)
|
NP_001374367.1:p.Ala168=
|
|
NM_001387440.1:c.*1365G>C
(CERS1)
|
NP_001374369.1:n.*1365G>C
|
|