ENST00000687337.1:c.*1689A>T
(AFG3L2)
|
ENSP00000508998.1:n.*1689A>T
|
|
ENST00000687477.1:n.629A>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.1955A>T
(AFG3L2)
|
ENSP00000510237.1:p.Asp652Val
|
|
ENST00000691179.1:c.2018A>T
(AFG3L2)
|
ENSP00000509010.1:p.Asp673Val
|
|
ENST00000691970.1:c.*1470A>T
(AFG3L2)
|
ENSP00000508440.1:n.*1470A>T
|
|
ENST00000692497.1:c.*523A>T
(AFG3L2)
|
ENSP00000509870.1:n.*523A>T
|
|
ENST00000692988.1:n.1911A>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2093A>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Asp698Val
|
|
ENST00000269143.7:c.2093A>T
(AFG3L2)
|
ENSP00000269143.2:p.Asp698Val
|
|
ENST00000586691.1:c.88-6626T>A
(TUBB6)
|
|
|
NM_006796.2:c.2093A>T , LRG_666t1:c.2093A>T
(AFG3L2)
|
NP_006787.2:p.Asp698Val
|
|
XM_011525601.1:c.1892A>T
(AFG3L2)
|
XP_011523903.1:p.Asp631Val
|
|
XM_011525601.3:c.1892A>T
(AFG3L2)
|
XP_011523903.1:p.Asp631Val
|
|
XR_002958227.1:n.451+521T>A
|
|
|
NM_006796.3:c.2093A>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Asp698Val
|
|