ENST00000687337.1:c.*1693T>C
(AFG3L2)
|
ENSP00000508998.1:n.*1693T>C
|
|
ENST00000687477.1:n.633T>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.1959T>C
(AFG3L2)
|
ENSP00000510237.1:p.Asp653=
|
|
ENST00000691179.1:c.2022T>C
(AFG3L2)
|
ENSP00000509010.1:p.Asp674=
|
|
ENST00000691970.1:c.*1474T>C
(AFG3L2)
|
ENSP00000508440.1:n.*1474T>C
|
|
ENST00000692497.1:c.*527T>C
(AFG3L2)
|
ENSP00000509870.1:n.*527T>C
|
|
ENST00000692988.1:n.1915T>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2097T>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Asp699=
|
|
ENST00000269143.7:c.2097T>C
(AFG3L2)
|
ENSP00000269143.2:p.Asp699=
|
|
ENST00000586691.1:c.88-6630A>G
(TUBB6)
|
|
|
NM_006796.2:c.2097T>C , LRG_666t1:c.2097T>C
(AFG3L2)
|
NP_006787.2:p.Asp699=
|
|
XM_011525601.1:c.1896T>C
(AFG3L2)
|
XP_011523903.1:p.Asp632=
|
|
XM_011525601.3:c.1896T>C
(AFG3L2)
|
XP_011523903.1:p.Asp632=
|
|
XR_002958227.1:n.451+517A>G
|
|
|
NM_006796.3:c.2097T>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Asp699=
|
|