ENST00000687337.1:c.*1577-276G>T
(AFG3L2)
|
ENSP00000508998.1:n.*1577-276G>T
|
|
ENST00000687477.1:n.517-276G>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.1843-276G>T
(AFG3L2)
|
ENSP00000510237.1:n.1843-276G>T
|
|
ENST00000691179.1:c.1906-276G>T
(AFG3L2)
|
ENSP00000509010.1:n.1906-276G>T
|
|
ENST00000691970.1:c.*1358-276G>T
(AFG3L2)
|
ENSP00000508440.1:n.*1358-276G>T
|
|
ENST00000692497.1:c.*411-276G>T
(AFG3L2)
|
ENSP00000509870.1:n.*411-276G>T
|
|
ENST00000692988.1:n.1799-276G>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.1981-276G>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:n.1981-276G>T
|
|
ENST00000269143.7:c.1981-276G>T
(AFG3L2)
|
ENSP00000269143.2:n.1981-276G>T
|
|
ENST00000586691.1:c.88-6238C>A
(TUBB6)
|
|
|
NM_006796.2:c.1981-276G>T , LRG_666t1:c.1981-276G>T
(AFG3L2)
|
NP_006787.2:n.1981-276G>T
|
|
XM_011525601.1:c.1780-276G>T
(AFG3L2)
|
XP_011523903.1:n.1780-276G>T
|
|
XM_011525601.3:c.1780-276G>T
(AFG3L2)
|
XP_011523903.1:n.1780-276G>T
|
|
XR_002958227.1:n.451+909C>A
|
|
|
NM_006796.3:c.1981-276G>T
(AFG3L2)
MANE Select
|
NP_006787.2:n.1981-276G>T
|
|