ENST00000687337.1:c.*1742C>A
(AFG3L2)
|
ENSP00000508998.1:n.*1742C>A
|
|
ENST00000687477.1:n.682C>A
(AFG3L2)
|
|
|
ENST00000688199.1:c.2008C>A
(AFG3L2)
|
ENSP00000510237.1:p.Leu670Ile
|
|
ENST00000691179.1:c.2071C>A
(AFG3L2)
|
ENSP00000509010.1:p.Leu691Ile
|
|
ENST00000691970.1:c.*1523C>A
(AFG3L2)
|
ENSP00000508440.1:n.*1523C>A
|
|
ENST00000692497.1:c.*576C>A
(AFG3L2)
|
ENSP00000509870.1:n.*576C>A
|
|
ENST00000692988.1:n.1964C>A
(AFG3L2)
|
|
|
ENST00000269143.8:c.2146C>A
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Leu716Ile
|
|
ENST00000269143.7:c.2146C>A
(AFG3L2)
|
ENSP00000269143.2:p.Leu716Ile
|
|
ENST00000586691.1:c.88-6679G>T
(TUBB6)
|
|
|
NM_006796.2:c.2146C>A , LRG_666t1:c.2146C>A
(AFG3L2)
|
NP_006787.2:p.Leu716Ile
|
|
XM_011525601.1:c.1945C>A
(AFG3L2)
|
XP_011523903.1:p.Leu649Ile
|
|
XM_011525601.3:c.1945C>A
(AFG3L2)
|
XP_011523903.1:p.Leu649Ile
|
|
XR_002958227.1:n.451+468G>T
|
|
|
NM_006796.3:c.2146C>A
(AFG3L2)
MANE Select
|
NP_006787.2:p.Leu716Ile
|
|