ENST00000687337.1:c.*1684G>A
(AFG3L2)
|
ENSP00000508998.1:n.*1684G>A
|
|
ENST00000687477.1:n.624G>A
(AFG3L2)
|
|
|
ENST00000688199.1:c.1950G>A
(AFG3L2)
|
ENSP00000510237.1:p.Leu650=
|
|
ENST00000691179.1:c.2013G>A
(AFG3L2)
|
ENSP00000509010.1:p.Leu671=
|
|
ENST00000691970.1:c.*1465G>A
(AFG3L2)
|
ENSP00000508440.1:n.*1465G>A
|
|
ENST00000692497.1:c.*518G>A
(AFG3L2)
|
ENSP00000509870.1:n.*518G>A
|
|
ENST00000692988.1:n.1906G>A
(AFG3L2)
|
|
|
ENST00000269143.8:c.2088G>A
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Leu696=
|
|
ENST00000269143.7:c.2088G>A
(AFG3L2)
|
ENSP00000269143.2:p.Leu696=
|
|
ENST00000586691.1:c.88-6621C>T
(TUBB6)
|
|
|
NM_006796.2:c.2088G>A , LRG_666t1:c.2088G>A
(AFG3L2)
|
NP_006787.2:p.Leu696=
|
|
XM_011525601.1:c.1887G>A
(AFG3L2)
|
XP_011523903.1:p.Leu629=
|
|
XM_011525601.3:c.1887G>A
(AFG3L2)
|
XP_011523903.1:p.Leu629=
|
|
XR_002958227.1:n.451+526C>T
|
|
|
NM_006796.3:c.2088G>A
(AFG3L2)
MANE Select
|
NP_006787.2:p.Leu696=
|
|