ENST00000378802.5:c.1332C>T
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Phe444=
|
|
ENST00000378802.4:c.1332C>T
(CYP4V2)
|
ENSP00000368079.4:p.Phe444=
|
|
ENST00000502665.1:n.567C>T
(CYP4V2)
|
|
|
ENST00000507209.5:n.6030C>T
(CYP4V2)
|
|
|
ENST00000511608.5:c.128C>T
(KLKB1)
|
|
|
ENST00000513354.5:n.422C>T
(CYP4V2)
|
|
|
NM_207352.3:c.1332C>T
(CYP4V2)
|
NP_997235.3:p.Phe444=
|
|
XM_005262935.2:c.1329C>T
(CYP4V2)
|
XP_005262992.1:p.Phe443=
|
|
XM_006714184.2:c.936C>T
(CYP4V2)
|
XP_006714247.1:p.Phe312=
|
|
XM_005262935.4:c.1329C>T
(CYP4V2)
|
XP_005262992.1:p.Phe443=
|
|
XM_017008037.1:c.936C>T
(CYP4V2)
|
XP_016863526.1:p.Phe312=
|
|
NM_207352.4:c.1332C>T
(CYP4V2)
MANE Select
|
NP_997235.3:p.Phe444=
|
|