ENST00000687337.1:c.*1683T>C
(AFG3L2)
|
ENSP00000508998.1:n.*1683T>C
|
|
ENST00000687477.1:n.623T>C
(AFG3L2)
|
|
|
ENST00000688199.1:c.1949T>C
(AFG3L2)
|
ENSP00000510237.1:p.Leu650Ser
|
|
ENST00000691179.1:c.2012T>C
(AFG3L2)
|
ENSP00000509010.1:p.Leu671Ser
|
|
ENST00000691970.1:c.*1464T>C
(AFG3L2)
|
ENSP00000508440.1:n.*1464T>C
|
|
ENST00000692497.1:c.*517T>C
(AFG3L2)
|
ENSP00000509870.1:n.*517T>C
|
|
ENST00000692988.1:n.1905T>C
(AFG3L2)
|
|
|
ENST00000269143.8:c.2087T>C
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Leu696Ser
|
|
ENST00000269143.7:c.2087T>C
(AFG3L2)
|
ENSP00000269143.2:p.Leu696Ser
|
|
ENST00000586691.1:c.88-6620A>G
(TUBB6)
|
|
|
NM_006796.2:c.2087T>C , LRG_666t1:c.2087T>C
(AFG3L2)
|
NP_006787.2:p.Leu696Ser
|
|
XM_011525601.1:c.1886T>C
(AFG3L2)
|
XP_011523903.1:p.Leu629Ser
|
|
XM_011525601.3:c.1886T>C
(AFG3L2)
|
XP_011523903.1:p.Leu629Ser
|
|
XR_002958227.1:n.451+527A>G
|
|
|
NM_006796.3:c.2087T>C
(AFG3L2)
MANE Select
|
NP_006787.2:p.Leu696Ser
|
|