ENST00000623882.4:c.*754G>C
(CERS1)
MANE Select
|
ENSP00000485308.1:n.*754G>C
|
|
ENST00000247005.8:c.485G>C
(GDF1)
MANE Select
|
ENSP00000247005.5:p.Gly162Ala
|
|
ENST00000247005.7:c.485G>C
(GDF1)
|
ENSP00000247005.5:p.Gly162Ala
|
|
ENST00000623882.3:c.*754G>C
(CERS1)
|
ENSP00000485308.1:n.*754G>C
|
|
ENST00000623927.1:c.485G>C
(CERS1)
|
ENSP00000485582.1:p.Gly162Ala
|
|
NM_001492.5:c.485G>C
(GDF1)
|
NP_001483.3:p.Gly162Ala
|
|
NM_021267.4:c.*754G>C
(CERS1)
|
NP_067090.1:n.*754G>C
|
|
NM_001492.6:c.485G>C
(GDF1)
MANE Select
|
NP_001483.3:p.Gly162Ala
|
|
NM_021267.5:c.*754G>C
(CERS1)
MANE Select
|
NP_067090.1:n.*754G>C
|
|
NM_001387438.1:c.485G>C
(GDF1)
|
NP_001374367.1:p.Gly162Ala
|
|
NM_001387440.1:c.*1346G>C
(CERS1)
|
NP_001374369.1:n.*1346G>C
|
|