ENST00000524407.7:c.1341T>G
(DNAAF3)
MANE Select
|
ENSP00000432046.3:p.Pro447=
|
|
ENST00000391720.8:c.1482T>G
(DNAAF3)
|
ENSP00000375600.5:p.Pro494=
|
|
ENST00000455045.5:c.1179T>G
(DNAAF3)
|
ENSP00000394343.1:p.Pro393=
|
|
ENST00000524407.6:c.1341T>G
(DNAAF3)
|
ENSP00000432046.2:p.Pro447=
|
|
ENST00000527223.6:c.1542T>G
(DNAAF3)
|
ENSP00000436975.2:p.Pro514=
|
|
ENST00000528412.5:c.*1129T>G
(DNAAF3)
|
ENSP00000433826.2:n.*1129T>G
|
|
ENST00000533527.6:n.1103T>G
(DNAAF3)
|
|
|
ENST00000587789.2:n.426T>G
(DNAAF3)
|
|
|
ENST00000587871.1:c.325T>G
|
|
|
ENST00000588076.1:c.340T>G
(DNAAF3)
|
|
|
NM_001256714.1:c.1542T>G
(DNAAF3)
|
NP_001243643.1:p.Pro514=
|
|
NM_001256715.1:c.1341T>G
(DNAAF3)
|
NP_001243644.1:p.Pro447=
|
|
NM_001256716.1:c.1179T>G
(DNAAF3)
|
NP_001243645.1:p.Pro393=
|
|
NM_178837.4:c.1482T>G
(DNAAF3)
|
NP_849159.2:p.Pro494=
|
|
XR_001754015.1:n.9A>C
(DNAAF3-AS1)
|
|
|
NM_001256715.2:c.1341T>G
(DNAAF3)
MANE Select
|
NP_001243644.1:p.Pro447=
|
|
NM_001256716.2:c.1179T>G
(DNAAF3)
|
NP_001243645.1:p.Pro393=
|
|