ENST00000248899.11:c.184T>G
(NCF4)
MANE Select
|
ENSP00000248899.6:p.Phe62Val
|
|
ENST00000397147.7:c.184T>G
(NCF4)
|
ENSP00000380334.4:p.Phe62Val
|
|
ENST00000650698.1:c.-126T>G
(NCF4)
|
ENSP00000498381.1:n.-126T>G
|
|
ENST00000650827.1:c.-126T>G
(NCF4)
|
ENSP00000498212.1:n.-126T>G
|
|
ENST00000651053.1:n.489T>G
(NCF4)
|
|
|
ENST00000248899.10:c.184T>G
(NCF4)
|
ENSP00000248899.6:p.Phe62Val
|
|
ENST00000397147.6:c.184T>G
(NCF4)
|
ENSP00000380334.4:p.Phe62Val
|
|
ENST00000447071.5:c.-126T>G
(NCF4)
|
ENSP00000414958.1:n.-126T>G
|
|
NM_000631.4:c.184T>G
(NCF4)
|
NP_000622.2:p.Phe62Val
|
|
NM_013416.3:c.184T>G , LRG_159t1:c.184T>G
(NCF4)
|
NP_038202.2:p.Phe62Val
|
|
XM_011530198.1:c.358T>G
(NCF4)
|
XP_011528500.1:p.Phe120Val
|
|
XM_011530199.1:c.328T>G
(NCF4)
|
XP_011528501.1:p.Phe110Val
|
|
NR_147197.1:n.351+5108A>C
(NCF4-AS1)
|
|
|
XM_017028808.1:c.-126T>G
(NCF4)
|
XP_016884297.1:n.-126T>G
|
|
NM_000631.5:c.184T>G
(NCF4)
MANE Select
|
NP_000622.2:p.Phe62Val
|
|
NM_013416.4:c.184T>G
(NCF4)
|
NP_038202.2:p.Phe62Val
|
|