ENST00000687337.1:c.*1727A>T
(AFG3L2)
|
ENSP00000508998.1:n.*1727A>T
|
|
ENST00000687477.1:n.667A>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.1993A>T
(AFG3L2)
|
ENSP00000510237.1:p.Arg665Ter
|
|
ENST00000691179.1:c.2056A>T
(AFG3L2)
|
ENSP00000509010.1:p.Arg686Ter
|
|
ENST00000691970.1:c.*1508A>T
(AFG3L2)
|
ENSP00000508440.1:n.*1508A>T
|
|
ENST00000692497.1:c.*561A>T
(AFG3L2)
|
ENSP00000509870.1:n.*561A>T
|
|
ENST00000692988.1:n.1949A>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2131A>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Arg711Ter
|
|
ENST00000269143.7:c.2131A>T
(AFG3L2)
|
ENSP00000269143.2:p.Arg711Ter
|
|
ENST00000586691.1:c.88-6664T>A
(TUBB6)
|
|
|
NM_006796.2:c.2131A>T , LRG_666t1:c.2131A>T
(AFG3L2)
|
NP_006787.2:p.Arg711Ter
|
|
XM_011525601.1:c.1930A>T
(AFG3L2)
|
XP_011523903.1:p.Arg644Ter
|
|
XM_011525601.3:c.1930A>T
(AFG3L2)
|
XP_011523903.1:p.Arg644Ter
|
|
XR_002958227.1:n.451+483T>A
|
|
|
NM_006796.3:c.2131A>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Arg711Ter
|
|