ENST00000248899.11:c.177C>A
(NCF4)
MANE Select
|
ENSP00000248899.6:p.Tyr59Ter
|
|
ENST00000397147.7:c.177C>A
(NCF4)
|
ENSP00000380334.4:p.Tyr59Ter
|
|
ENST00000650698.1:c.-133C>A
(NCF4)
|
ENSP00000498381.1:n.-133C>A
|
|
ENST00000650827.1:c.-133C>A
(NCF4)
|
ENSP00000498212.1:n.-133C>A
|
|
ENST00000651053.1:n.482C>A
(NCF4)
|
|
|
ENST00000248899.10:c.177C>A
(NCF4)
|
ENSP00000248899.6:p.Tyr59Ter
|
|
ENST00000397147.6:c.177C>A
(NCF4)
|
ENSP00000380334.4:p.Tyr59Ter
|
|
ENST00000447071.5:c.-133C>A
(NCF4)
|
ENSP00000414958.1:n.-133C>A
|
|
NM_000631.4:c.177C>A
(NCF4)
|
NP_000622.2:p.Tyr59Ter
|
|
NM_013416.3:c.177C>A , LRG_159t1:c.177C>A
(NCF4)
|
NP_038202.2:p.Tyr59Ter
|
|
XM_011530198.1:c.351C>A
(NCF4)
|
XP_011528500.1:p.Tyr117Ter
|
|
XM_011530199.1:c.321C>A
(NCF4)
|
XP_011528501.1:p.Tyr107Ter
|
|
NR_147197.1:n.351+5115G>T
(NCF4-AS1)
|
|
|
XM_017028808.1:c.-133C>A
(NCF4)
|
XP_016884297.1:n.-133C>A
|
|
NM_000631.5:c.177C>A
(NCF4)
MANE Select
|
NP_000622.2:p.Tyr59Ter
|
|
NM_013416.4:c.177C>A
(NCF4)
|
NP_038202.2:p.Tyr59Ter
|
|