ENST00000248899.11:c.139A>T
(NCF4)
MANE Select
|
ENSP00000248899.6:p.Thr47Ser
|
|
ENST00000397147.7:c.139A>T
(NCF4)
|
ENSP00000380334.4:p.Thr47Ser
|
|
ENST00000650698.1:c.-171A>T
(NCF4)
|
ENSP00000498381.1:n.-171A>T
|
|
ENST00000650827.1:c.-171A>T
(NCF4)
|
ENSP00000498212.1:n.-171A>T
|
|
ENST00000651053.1:n.444A>T
(NCF4)
|
|
|
ENST00000248899.10:c.139A>T
(NCF4)
|
ENSP00000248899.6:p.Thr47Ser
|
|
ENST00000397147.6:c.139A>T
(NCF4)
|
ENSP00000380334.4:p.Thr47Ser
|
|
ENST00000447071.5:c.-171A>T
(NCF4)
|
ENSP00000414958.1:n.-171A>T
|
|
NM_000631.4:c.139A>T
(NCF4)
|
NP_000622.2:p.Thr47Ser
|
|
NM_013416.3:c.139A>T , LRG_159t1:c.139A>T
(NCF4)
|
NP_038202.2:p.Thr47Ser
|
|
XM_011530198.1:c.313A>T
(NCF4)
|
XP_011528500.1:p.Thr105Ser
|
|
XM_011530199.1:c.283A>T
(NCF4)
|
XP_011528501.1:p.Thr95Ser
|
|
NR_147197.1:n.351+5153T>A
(NCF4-AS1)
|
|
|
XM_017028808.1:c.-171A>T
(NCF4)
|
XP_016884297.1:n.-171A>T
|
|
NM_000631.5:c.139A>T
(NCF4)
MANE Select
|
NP_000622.2:p.Thr47Ser
|
|
NM_013416.4:c.139A>T
(NCF4)
|
NP_038202.2:p.Thr47Ser
|
|