ENST00000687337.1:c.*1758C>T
(AFG3L2)
|
ENSP00000508998.1:n.*1758C>T
|
|
ENST00000687477.1:n.698C>T
(AFG3L2)
|
|
|
ENST00000688199.1:c.2024C>T
(AFG3L2)
|
ENSP00000510237.1:p.Ala675Val
|
|
ENST00000691179.1:c.2087C>T
(AFG3L2)
|
ENSP00000509010.1:p.Ala696Val
|
|
ENST00000691970.1:c.*1539C>T
(AFG3L2)
|
ENSP00000508440.1:n.*1539C>T
|
|
ENST00000692497.1:c.*592C>T
(AFG3L2)
|
ENSP00000509870.1:n.*592C>T
|
|
ENST00000692988.1:n.1980C>T
(AFG3L2)
|
|
|
ENST00000269143.8:c.2162C>T
(AFG3L2)
MANE Select
|
ENSP00000269143.2:p.Ala721Val
|
|
ENST00000269143.7:c.2162C>T
(AFG3L2)
|
ENSP00000269143.2:p.Ala721Val
|
|
ENST00000586691.1:c.88-6695G>A
(TUBB6)
|
|
|
NM_006796.2:c.2162C>T , LRG_666t1:c.2162C>T
(AFG3L2)
|
NP_006787.2:p.Ala721Val
|
|
XM_011525601.1:c.1961C>T
(AFG3L2)
|
XP_011523903.1:p.Ala654Val
|
|
XM_011525601.3:c.1961C>T
(AFG3L2)
|
XP_011523903.1:p.Ala654Val
|
|
XR_002958227.1:n.451+452G>A
|
|
|
NM_006796.3:c.2162C>T
(AFG3L2)
MANE Select
|
NP_006787.2:p.Ala721Val
|
|