ENST00000687337.1:c.*1721T>C
(AFG3L2)
|
ENSP00000508998.1:n.*1721T>C
|
|
ENST00000687477.1:n.661T>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.1987T>C
(AFG3L2)
|
ENSP00000510237.1:p.Tyr663His
|
|
ENST00000691179.1:c.2050T>C
(AFG3L2)
|
ENSP00000509010.1:p.Tyr684His
|
|
ENST00000691970.1:c.*1502T>C
(AFG3L2)
|
ENSP00000508440.1:n.*1502T>C
|
|
ENST00000692497.1:c.*555T>C
(AFG3L2)
|
ENSP00000509870.1:n.*555T>C
|
|
ENST00000692988.1:n.1943T>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2125T>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Tyr709His
|
|
ENST00000269143.7:c.2125T>C
(AFG3L2)
|
ENSP00000269143.2:p.Tyr709His
|
|
ENST00000586691.1:c.88-6658A>G
(TUBB6)
|
|
|
NM_006796.2:c.2125T>C , LRG_666t1:c.2125T>C
(AFG3L2)
|
NP_006787.2:p.Tyr709His
|
|
XM_011525601.1:c.1924T>C
(AFG3L2)
|
XP_011523903.1:p.Tyr642His
|
|
XM_011525601.3:c.1924T>C
(AFG3L2)
|
XP_011523903.1:p.Tyr642His
|
|
XR_002958227.1:n.451+489A>G
|
|
|
NM_006796.3:c.2125T>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Tyr709His
|
|