ENST00000378802.5:c.1414T>G
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Phe472Val
|
|
ENST00000378802.4:c.1414T>G
(CYP4V2)
|
ENSP00000368079.4:p.Phe472Val
|
|
ENST00000502665.1:n.649T>G
(CYP4V2)
|
|
|
ENST00000507209.5:n.6112T>G
(CYP4V2)
|
|
|
ENST00000511608.5:c.201+1205T>G
(KLKB1)
|
|
|
ENST00000513354.5:n.504T>G
(CYP4V2)
|
|
|
NM_207352.3:c.1414T>G
(CYP4V2)
|
NP_997235.3:p.Phe472Val
|
|
XM_005262935.2:c.1411T>G
(CYP4V2)
|
XP_005262992.1:p.Phe471Val
|
|
XM_006714184.2:c.1018T>G
(CYP4V2)
|
XP_006714247.1:p.Phe340Val
|
|
XM_005262935.4:c.1411T>G
(CYP4V2)
|
XP_005262992.1:p.Phe471Val
|
|
XM_017008037.1:c.1018T>G
(CYP4V2)
|
XP_016863526.1:p.Phe340Val
|
|
NM_207352.4:c.1414T>G
(CYP4V2)
MANE Select
|
NP_997235.3:p.Phe472Val
|
|