ENST00000262134.10:c.1216-7808T>G
(LPCAT2)
MANE Select
|
ENSP00000262134.5:n.1216-7808T>G
|
|
ENST00000457326.3:c.67T>G
(CAPNS2)
MANE Select
|
ENSP00000400882.2:p.Phe23Val
|
|
ENST00000262134.9:c.1216-7808T>G
(LPCAT2)
|
ENSP00000262134.5:n.1216-7808T>G
|
|
ENST00000457326.2:c.67T>G
(CAPNS2)
|
ENSP00000400882.2:p.Phe23Val
|
|
ENST00000563095.5:n.614-7808T>G
(LPCAT2)
|
|
|
ENST00000565056.1:n.90-7808T>G
(LPCAT2)
|
|
|
ENST00000566915.5:n.1298-7808T>G
(LPCAT2)
|
|
|
ENST00000615823.1:c.340-7808T>G
(LPCAT2)
|
ENSP00000483225.1:n.340-7808T>G
|
|
NM_017839.4:c.1216-7808T>G
(LPCAT2)
|
NP_060309.2:n.1216-7808T>G
|
|
NM_032330.1:c.67T>G
(CAPNS2)
|
NP_115706.1:p.Phe23Val
|
|
XM_006721211.2:c.1048-7808T>G
(LPCAT2)
|
XP_006721274.1:n.1048-7808T>G
|
|
XM_011523169.1:c.406-7808T>G
(LPCAT2)
|
XP_011521471.1:n.406-7808T>G
|
|
NM_032330.2:c.67T>G
(CAPNS2)
|
NP_115706.1:p.Phe23Val
|
|
XM_011523169.3:c.406-7808T>G
(LPCAT2)
|
XP_011521471.1:n.406-7808T>G
|
|
XM_017023376.1:c.1048-7808T>G
(LPCAT2)
|
XP_016878865.1:n.1048-7808T>G
|
|
NM_017839.5:c.1216-7808T>G
(LPCAT2)
MANE Select
|
NP_060309.2:n.1216-7808T>G
|
|
NM_032330.3:c.67T>G
(CAPNS2)
MANE Select
|
NP_115706.1:p.Phe23Val
|
|