ENST00000687337.1:c.*1712A>C
(AFG3L2)
|
ENSP00000508998.1:n.*1712A>C
|
|
ENST00000687477.1:n.652A>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.1978A>C
(AFG3L2)
|
ENSP00000510237.1:p.Asn660His
|
|
ENST00000691179.1:c.2041A>C
(AFG3L2)
|
ENSP00000509010.1:p.Asn681His
|
|
ENST00000691970.1:c.*1493A>C
(AFG3L2)
|
ENSP00000508440.1:n.*1493A>C
|
|
ENST00000692497.1:c.*546A>C
(AFG3L2)
|
ENSP00000509870.1:n.*546A>C
|
|
ENST00000692988.1:n.1934A>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2116A>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Asn706His
|
|
ENST00000269143.7:c.2116A>C
(AFG3L2)
|
ENSP00000269143.2:p.Asn706His
|
|
ENST00000586691.1:c.88-6649T>G
(TUBB6)
|
|
|
NM_006796.2:c.2116A>C , LRG_666t1:c.2116A>C
(AFG3L2)
|
NP_006787.2:p.Asn706His
|
|
XM_011525601.1:c.1915A>C
(AFG3L2)
|
XP_011523903.1:p.Asn639His
|
|
XM_011525601.3:c.1915A>C
(AFG3L2)
|
XP_011523903.1:p.Asn639His
|
|
XR_002958227.1:n.451+498T>G
|
|
|
NM_006796.3:c.2116A>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Asn706His
|
|