ENST00000687337.1:c.*1748G=
(AFG3L2)
|
ENSP00000508998.1:n.*1748G=
|
|
ENST00000687477.1:n.688G=
(AFG3L2)
|
|
|
ENST00000688199.1:c.2014G=
(AFG3L2)
|
ENSP00000510237.1:p.Glu672=
|
|
ENST00000691179.1:c.2077G=
(AFG3L2)
|
ENSP00000509010.1:p.Glu693=
|
|
ENST00000691970.1:c.*1529G=
(AFG3L2)
|
ENSP00000508440.1:n.*1529G=
|
|
ENST00000692497.1:c.*582G=
(AFG3L2)
|
ENSP00000509870.1:n.*582G=
|
|
ENST00000692988.1:n.1970G=
(AFG3L2)
|
|
|
ENST00000269143.8:c.2152G=
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Glu718=
|
|
ENST00000269143.7:c.2152G=
(AFG3L2)
|
ENSP00000269143.2:p.Glu718=
|
|
ENST00000586691.1:c.88-6685C=
(TUBB6)
|
|
|
NM_006796.2:c.2152G= , LRG_666t1:c.2152G=
(AFG3L2)
|
NP_006787.2:p.Glu718=
|
|
XM_011525601.1:c.1951G=
(AFG3L2)
|
XP_011523903.1:p.Glu651=
|
|
XM_011525601.3:c.1951G=
(AFG3L2)
|
XP_011523903.1:p.Glu651=
|
|
XR_002958227.1:n.451+462C=
|
|
|
NM_006796.3:c.2152G=
(AFG3L2)
MANE Select
|
NP_006787.2:p.Glu718=
|
|