ENST00000321149.7:c.1235T>G
(DNAAF4)
MANE Select
|
ENSP00000323275.3:p.Val412Gly
|
|
ENST00000348518.4:c.1235T>G
(DNAAF4)
|
ENSP00000299561.5:p.Val412Gly
|
|
ENST00000448430.6:c.1047+4207T>G
(DNAAF4)
|
ENSP00000403412.2:n.1047+4207T>G
|
|
ENST00000457155.6:c.1129T>G
(DNAAF4)
|
ENSP00000402640.2:p.Ter377Glu
|
|
ENST00000524160.5:c.*480+1799T>G
(DNAAF4)
|
ENSP00000428097.1:n.*480+1799T>G
|
|
NM_001033559.2:c.1129T>G
(DNAAF4)
|
NP_001028731.1:p.Ter377Glu
|
|
NM_001033560.1:c.1047+4207T>G
(DNAAF4)
|
NP_001028732.1:n.1047+4207T>G
|
|
NM_130810.3:c.1235T>G
(DNAAF4)
|
NP_570722.2:p.Val412Gly
|
|
NR_037923.1:n.1408+1799T>G
(DNAAF4-CCPG1)
|
|
|
NM_130810.4:c.1235T>G
(DNAAF4)
MANE Select
|
NP_570722.2:p.Val412Gly
|
|
NM_001033559.3:c.1129T>G
(DNAAF4)
|
NP_001028731.1:p.Ter377Glu
|
|
NM_001033560.2:c.1047+4207T>G
(DNAAF4)
|
NP_001028732.1:n.1047+4207T>G
|
|