ENST00000292427.10:c.1455C>T
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Tyr485=
|
|
ENST00000292427.8:c.1455C>T
(CYP11B1)
|
ENSP00000292427.4:p.Tyr485=
|
|
ENST00000314111.4:n.1652C>T
(CYP11B1)
|
|
|
ENST00000377675.3:c.1668C>T
(CYP11B1)
|
ENSP00000366903.3:p.Tyr556=
|
|
ENST00000517471.5:c.1257C>T
(CYP11B1)
|
ENSP00000428043.1:p.Tyr419=
|
|
ENST00000519285.5:c.489C>T
(CYP11B1)
|
ENSP00000430144.1:p.Tyr163=
|
|
ENST00000522728.5:c.181+33205G>A
(GML)
|
ENSP00000430799.1:n.181+33205G>A
|
|
NM_000497.3:c.1455C>T
(CYP11B1)
|
NP_000488.3:p.Tyr485=
|
|
NM_001026213.1:c.1257C>T
(CYP11B1)
|
NP_001021384.1:p.Tyr419=
|
|
XM_011516870.1:c.1693C>T
(CYP11B1)
|
XP_011515172.1:p.Gln565Ter
|
|
XM_011516871.1:c.1624C>T
(CYP11B1)
|
XP_011515173.1:p.Gln542Ter
|
|
XM_011516872.1:c.1615C>T
(CYP11B1)
|
XP_011515174.1:p.Gln539Ter
|
|
XM_011516873.1:c.1602C>T
(CYP11B1)
|
XP_011515175.1:p.Tyr534=
|
|
XM_011516874.1:c.1533C>T
(CYP11B1)
|
XP_011515176.1:p.Tyr511=
|
|
XM_011516875.1:c.1432C>T
(CYP11B1)
|
XP_011515177.1:p.Gln478Ter
|
|
XM_011516876.1:c.1404C>T
(CYP11B1)
|
XP_011515178.1:p.Tyr468=
|
|
XM_011516970.1:c.214+33205G>A
(GML)
|
XP_011515272.1:n.214+33205G>A
|
|
NM_000497.4:c.1455C>T
(CYP11B1)
MANE Select
|
NP_000488.3:p.Tyr485=
|
|