ENST00000321149.7:c.1246A>T
(DNAAF4)
MANE Select
|
ENSP00000323275.3:p.Thr416Ser
|
|
ENST00000348518.4:c.1246A>T
(DNAAF4)
|
ENSP00000299561.5:p.Thr416Ser
|
|
ENST00000448430.6:c.1047+4218A>T
(DNAAF4)
|
ENSP00000403412.2:n.1047+4218A>T
|
|
ENST00000457155.6:c.*9A>T
(DNAAF4)
|
ENSP00000402640.2:n.*9A>T
|
|
ENST00000524160.5:c.*480+1810A>T
(DNAAF4)
|
ENSP00000428097.1:n.*480+1810A>T
|
|
NM_001033559.2:c.*9A>T
(DNAAF4)
|
NP_001028731.1:n.*9A>T
|
|
NM_001033560.1:c.1047+4218A>T
(DNAAF4)
|
NP_001028732.1:n.1047+4218A>T
|
|
NM_130810.3:c.1246A>T
(DNAAF4)
|
NP_570722.2:p.Thr416Ser
|
|
NR_037923.1:n.1408+1810A>T
(DNAAF4-CCPG1)
|
|
|
NM_130810.4:c.1246A>T
(DNAAF4)
MANE Select
|
NP_570722.2:p.Thr416Ser
|
|
NM_001033559.3:c.*9A>T
(DNAAF4)
|
NP_001028731.1:n.*9A>T
|
|
NM_001033560.2:c.1047+4218A>T
(DNAAF4)
|
NP_001028732.1:n.1047+4218A>T
|
|