ENST00000687337.1:c.*1741T>C
(AFG3L2)
|
ENSP00000508998.1:n.*1741T>C
|
|
ENST00000687477.1:n.681T>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.2007T>C
(AFG3L2)
|
ENSP00000510237.1:p.Leu669=
|
|
ENST00000691179.1:c.2070T>C
(AFG3L2)
|
ENSP00000509010.1:p.Leu690=
|
|
ENST00000691970.1:c.*1522T>C
(AFG3L2)
|
ENSP00000508440.1:n.*1522T>C
|
|
ENST00000692497.1:c.*575T>C
(AFG3L2)
|
ENSP00000509870.1:n.*575T>C
|
|
ENST00000692988.1:n.1963T>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2145T>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Leu715=
|
|
ENST00000269143.7:c.2145T>C
(AFG3L2)
|
ENSP00000269143.2:p.Leu715=
|
|
ENST00000586691.1:c.88-6678A>G
(TUBB6)
|
|
|
NM_006796.2:c.2145T>C , LRG_666t1:c.2145T>C
(AFG3L2)
|
NP_006787.2:p.Leu715=
|
|
XM_011525601.1:c.1944T>C
(AFG3L2)
|
XP_011523903.1:p.Leu648=
|
|
XM_011525601.3:c.1944T>C
(AFG3L2)
|
XP_011523903.1:p.Leu648=
|
|
XR_002958227.1:n.451+469A>G
|
|
|
NM_006796.3:c.2145T>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Leu715=
|
|