ENST00000687337.1:c.*1744C>T
(AFG3L2)
|
ENSP00000508998.1:n.*1744C>T
|
|
ENST00000687477.1:n.684C>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.2010C>T
(AFG3L2)
|
ENSP00000510237.1:p.Leu670=
|
|
ENST00000691179.1:c.2073C>T
(AFG3L2)
|
ENSP00000509010.1:p.Leu691=
|
|
ENST00000691970.1:c.*1525C>T
(AFG3L2)
|
ENSP00000508440.1:n.*1525C>T
|
|
ENST00000692497.1:c.*578C>T
(AFG3L2)
|
ENSP00000509870.1:n.*578C>T
|
|
ENST00000692988.1:n.1966C>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2148C>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Leu716=
|
|
ENST00000269143.7:c.2148C>T
(AFG3L2)
|
ENSP00000269143.2:p.Leu716=
|
|
ENST00000586691.1:c.88-6681G>A
(TUBB6)
|
|
|
NM_006796.2:c.2148C>T , LRG_666t1:c.2148C>T
(AFG3L2)
|
NP_006787.2:p.Leu716=
|
|
XM_011525601.1:c.1947C>T
(AFG3L2)
|
XP_011523903.1:p.Leu649=
|
|
XM_011525601.3:c.1947C>T
(AFG3L2)
|
XP_011523903.1:p.Leu649=
|
|
XR_002958227.1:n.451+466G>A
|
|
|
NM_006796.3:c.2148C>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Leu716=
|
|