ENST00000292427.10:c.724A>C
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Arg242=
|
|
ENST00000292427.8:c.724A>C
(CYP11B1)
|
ENSP00000292427.4:p.Arg242=
|
|
ENST00000314111.4:n.757A>C
(CYP11B1)
|
|
|
ENST00000377675.3:c.937A>C
(CYP11B1)
|
ENSP00000366903.3:p.Arg313=
|
|
ENST00000517471.5:c.724A>C
(CYP11B1)
|
ENSP00000428043.1:p.Arg242=
|
|
ENST00000522728.5:c.181+35532T>G
(GML)
|
ENSP00000430799.1:n.181+35532T>G
|
|
NM_000497.3:c.724A>C
(CYP11B1)
|
NP_000488.3:p.Arg242=
|
|
NM_001026213.1:c.724A>C
(CYP11B1)
|
NP_001021384.1:p.Arg242=
|
|
XM_011516870.1:c.802A>C
(CYP11B1)
|
XP_011515172.1:p.Arg268=
|
|
XM_011516871.1:c.802A>C
(CYP11B1)
|
XP_011515173.1:p.Arg268=
|
|
XM_011516872.1:c.724A>C
(CYP11B1)
|
XP_011515174.1:p.Arg242=
|
|
XM_011516873.1:c.802A>C
(CYP11B1)
|
XP_011515175.1:p.Arg268=
|
|
XM_011516874.1:c.802A>C
(CYP11B1)
|
XP_011515176.1:p.Arg268=
|
|
XM_011516875.1:c.541A>C
(CYP11B1)
|
XP_011515177.1:p.Arg181=
|
|
XM_011516876.1:c.802A>C
(CYP11B1)
|
XP_011515178.1:p.Arg268=
|
|
XM_011516970.1:c.214+35532T>G
(GML)
|
XP_011515272.1:n.214+35532T>G
|
|
NM_000497.4:c.724A>C
(CYP11B1)
MANE Select
|
NP_000488.3:p.Arg242=
|
|