ENST00000687337.1:c.*1730A>T
(AFG3L2)
|
ENSP00000508998.1:n.*1730A>T
|
|
ENST00000687477.1:n.670A>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.1996A>T
(AFG3L2)
|
ENSP00000510237.1:p.Thr666Ser
|
|
ENST00000691179.1:c.2059A>T
(AFG3L2)
|
ENSP00000509010.1:p.Thr687Ser
|
|
ENST00000691970.1:c.*1511A>T
(AFG3L2)
|
ENSP00000508440.1:n.*1511A>T
|
|
ENST00000692497.1:c.*564A>T
(AFG3L2)
|
ENSP00000509870.1:n.*564A>T
|
|
ENST00000692988.1:n.1952A>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2134A>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Thr712Ser
|
|
ENST00000269143.7:c.2134A>T
(AFG3L2)
|
ENSP00000269143.2:p.Thr712Ser
|
|
ENST00000586691.1:c.88-6667T>A
(TUBB6)
|
|
|
NM_006796.2:c.2134A>T , LRG_666t1:c.2134A>T
(AFG3L2)
|
NP_006787.2:p.Thr712Ser
|
|
XM_011525601.1:c.1933A>T
(AFG3L2)
|
XP_011523903.1:p.Thr645Ser
|
|
XM_011525601.3:c.1933A>T
(AFG3L2)
|
XP_011523903.1:p.Thr645Ser
|
|
XR_002958227.1:n.451+480T>A
|
|
|
NM_006796.3:c.2134A>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Thr712Ser
|
|