ENST00000378802.5:c.1238T>C
(CYP4V2)
MANE Select
|
ENSP00000368079.4:p.Val413Ala
|
|
ENST00000378802.4:c.1238T>C
(CYP4V2)
|
ENSP00000368079.4:p.Val413Ala
|
|
ENST00000502665.1:n.473T>C
(CYP4V2)
|
|
|
ENST00000507209.5:n.5936T>C
(CYP4V2)
|
|
|
ENST00000511608.5:c.34T>C
(KLKB1)
|
|
|
ENST00000513354.5:n.328T>C
(CYP4V2)
|
|
|
NM_207352.3:c.1238T>C
(CYP4V2)
|
NP_997235.3:p.Val413Ala
|
|
XM_005262935.2:c.1235T>C
(CYP4V2)
|
XP_005262992.1:p.Val412Ala
|
|
XM_006714184.2:c.842T>C
(CYP4V2)
|
XP_006714247.1:p.Val281Ala
|
|
XM_005262935.4:c.1235T>C
(CYP4V2)
|
XP_005262992.1:p.Val412Ala
|
|
XM_017008037.1:c.842T>C
(CYP4V2)
|
XP_016863526.1:p.Val281Ala
|
|
NM_207352.4:c.1238T>C
(CYP4V2)
MANE Select
|
NP_997235.3:p.Val413Ala
|
|