ENST00000687337.1:c.*1678A>G
(AFG3L2)
|
ENSP00000508998.1:n.*1678A>G
|
|
ENST00000687477.1:n.618A>G
(AFG3L2)
|
|
|
ENST00000688199.1:c.1944A>G
(AFG3L2)
|
ENSP00000510237.1:p.Ala648=
|
|
ENST00000691179.1:c.2007A>G
(AFG3L2)
|
ENSP00000509010.1:p.Ala669=
|
|
ENST00000691970.1:c.*1459A>G
(AFG3L2)
|
ENSP00000508440.1:n.*1459A>G
|
|
ENST00000692497.1:c.*512A>G
(AFG3L2)
|
ENSP00000509870.1:n.*512A>G
|
|
ENST00000692988.1:n.1900A>G
(AFG3L2)
|
|
|
ENST00000269143.8:c.2082A>G
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Ala694=
|
|
ENST00000269143.7:c.2082A>G
(AFG3L2)
|
ENSP00000269143.2:p.Ala694=
|
|
ENST00000586691.1:c.88-6615T>C
(TUBB6)
|
|
|
NM_006796.2:c.2082A>G , LRG_666t1:c.2082A>G
(AFG3L2)
|
NP_006787.2:p.Ala694=
|
|
XM_011525601.1:c.1881A>G
(AFG3L2)
|
XP_011523903.1:p.Ala627=
|
|
XM_011525601.3:c.1881A>G
(AFG3L2)
|
XP_011523903.1:p.Ala627=
|
|
XR_002958227.1:n.451+532T>C
|
|
|
NM_006796.3:c.2082A>G
(AFG3L2)
MANE Select
|
NP_006787.2:p.Ala694=
|
|