ENST00000687337.1:c.*1645G>T
(AFG3L2)
|
ENSP00000508998.1:n.*1645G>T
|
|
ENST00000687477.1:n.585G>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.1911G>T
(AFG3L2)
|
ENSP00000510237.1:p.Met637Ile
|
|
ENST00000691179.1:c.1974G>T
(AFG3L2)
|
ENSP00000509010.1:p.Met658Ile
|
|
ENST00000691970.1:c.*1426G>T
(AFG3L2)
|
ENSP00000508440.1:n.*1426G>T
|
|
ENST00000692497.1:c.*479G>T
(AFG3L2)
|
ENSP00000509870.1:n.*479G>T
|
|
ENST00000692988.1:n.1867G>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2049G>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Met683Ile
|
|
ENST00000269143.7:c.2049G>T
(AFG3L2)
|
ENSP00000269143.2:p.Met683Ile
|
|
ENST00000586691.1:c.88-6582C>A
(TUBB6)
|
|
|
NM_006796.2:c.2049G>T , LRG_666t1:c.2049G>T
(AFG3L2)
|
NP_006787.2:p.Met683Ile
|
|
XM_011525601.1:c.1848G>T
(AFG3L2)
|
XP_011523903.1:p.Met616Ile
|
|
XM_011525601.3:c.1848G>T
(AFG3L2)
|
XP_011523903.1:p.Met616Ile
|
|
XR_002958227.1:n.451+565C>A
|
|
|
NM_006796.3:c.2049G>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Met683Ile
|
|