ENST00000687337.1:c.*1700C>G
(AFG3L2)
|
ENSP00000508998.1:n.*1700C>G
|
|
ENST00000687477.1:n.640C>G
(AFG3L2)
|
|
|
ENST00000688199.1:c.1966C>G
(AFG3L2)
|
ENSP00000510237.1:p.Arg656Gly
|
|
ENST00000691179.1:c.2029C>G
(AFG3L2)
|
ENSP00000509010.1:p.Arg677Gly
|
|
ENST00000691970.1:c.*1481C>G
(AFG3L2)
|
ENSP00000508440.1:n.*1481C>G
|
|
ENST00000692497.1:c.*534C>G
(AFG3L2)
|
ENSP00000509870.1:n.*534C>G
|
|
ENST00000692988.1:n.1922C>G
(AFG3L2)
|
|
|
ENST00000269143.8:c.2104C>G
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Arg702Gly
|
|
ENST00000269143.7:c.2104C>G
(AFG3L2)
|
ENSP00000269143.2:p.Arg702Gly
|
|
ENST00000586691.1:c.88-6637G>C
(TUBB6)
|
|
|
NM_006796.2:c.2104C>G , LRG_666t1:c.2104C>G
(AFG3L2)
|
NP_006787.2:p.Arg702Gly
|
|
XM_011525601.1:c.1903C>G
(AFG3L2)
|
XP_011523903.1:p.Arg635Gly
|
|
XM_011525601.3:c.1903C>G
(AFG3L2)
|
XP_011523903.1:p.Arg635Gly
|
|
XR_002958227.1:n.451+510G>C
|
|
|
NM_006796.3:c.2104C>G
(AFG3L2)
MANE Select
|
NP_006787.2:p.Arg702Gly
|
|