ENST00000292427.10:c.1464A>G
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Ile488Met
|
|
ENST00000292427.8:c.1464A>G
(CYP11B1)
|
ENSP00000292427.4:p.Ile488Met
|
|
ENST00000314111.4:n.1661A>G
(CYP11B1)
|
|
|
ENST00000377675.3:c.1677A>G
(CYP11B1)
|
ENSP00000366903.3:p.Ile559Met
|
|
ENST00000517471.5:c.1266A>G
(CYP11B1)
|
ENSP00000428043.1:p.Ile422Met
|
|
ENST00000519285.5:c.498A>G
(CYP11B1)
|
ENSP00000430144.1:p.Ile166Met
|
|
ENST00000522728.5:c.181+33196T>C
(GML)
|
ENSP00000430799.1:n.181+33196T>C
|
|
NM_000497.3:c.1464A>G
(CYP11B1)
|
NP_000488.3:p.Ile488Met
|
|
NM_001026213.1:c.1266A>G
(CYP11B1)
|
NP_001021384.1:p.Ile422Met
|
|
XM_011516870.1:c.1702A>G
(CYP11B1)
|
XP_011515172.1:p.Ile568Val
|
|
XM_011516871.1:c.1633A>G
(CYP11B1)
|
XP_011515173.1:p.Ile545Val
|
|
XM_011516872.1:c.1624A>G
(CYP11B1)
|
XP_011515174.1:p.Ile542Val
|
|
XM_011516873.1:c.1611A>G
(CYP11B1)
|
XP_011515175.1:p.Ile537Met
|
|
XM_011516874.1:c.1542A>G
(CYP11B1)
|
XP_011515176.1:p.Ile514Met
|
|
XM_011516875.1:c.1441A>G
(CYP11B1)
|
XP_011515177.1:p.Ile481Val
|
|
XM_011516876.1:c.1413A>G
(CYP11B1)
|
XP_011515178.1:p.Ile471Met
|
|
XM_011516970.1:c.214+33196T>C
(GML)
|
XP_011515272.1:n.214+33196T>C
|
|
NM_000497.4:c.1464A>G
(CYP11B1)
MANE Select
|
NP_000488.3:p.Ile488Met
|
|