ENST00000687337.1:c.*1715G>C
(AFG3L2)
|
ENSP00000508998.1:n.*1715G>C
|
|
ENST00000687477.1:n.655G>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.1981G>C
(AFG3L2)
|
ENSP00000510237.1:p.Asp661His
|
|
ENST00000691179.1:c.2044G>C
(AFG3L2)
|
ENSP00000509010.1:p.Asp682His
|
|
ENST00000691970.1:c.*1496G>C
(AFG3L2)
|
ENSP00000508440.1:n.*1496G>C
|
|
ENST00000692497.1:c.*549G>C
(AFG3L2)
|
ENSP00000509870.1:n.*549G>C
|
|
ENST00000692988.1:n.1937G>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2119G>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Asp707His
|
|
ENST00000269143.7:c.2119G>C
(AFG3L2)
|
ENSP00000269143.2:p.Asp707His
|
|
ENST00000586691.1:c.88-6652C>G
(TUBB6)
|
|
|
NM_006796.2:c.2119G>C , LRG_666t1:c.2119G>C
(AFG3L2)
|
NP_006787.2:p.Asp707His
|
|
XM_011525601.1:c.1918G>C
(AFG3L2)
|
XP_011523903.1:p.Asp640His
|
|
XM_011525601.3:c.1918G>C
(AFG3L2)
|
XP_011523903.1:p.Asp640His
|
|
XR_002958227.1:n.451+495C>G
|
|
|
NM_006796.3:c.2119G>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Asp707His
|
|