ENST00000292427.10:c.1461C>A
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Phe487Leu
|
|
ENST00000292427.8:c.1461C>A
(CYP11B1)
|
ENSP00000292427.4:p.Phe487Leu
|
|
ENST00000314111.4:n.1658C>A
(CYP11B1)
|
|
|
ENST00000377675.3:c.1674C>A
(CYP11B1)
|
ENSP00000366903.3:p.Phe558Leu
|
|
ENST00000517471.5:c.1263C>A
(CYP11B1)
|
ENSP00000428043.1:p.Phe421Leu
|
|
ENST00000519285.5:c.495C>A
(CYP11B1)
|
ENSP00000430144.1:p.Phe165Leu
|
|
ENST00000522728.5:c.181+33199G>T
(GML)
|
ENSP00000430799.1:n.181+33199G>T
|
|
NM_000497.3:c.1461C>A
(CYP11B1)
|
NP_000488.3:p.Phe487Leu
|
|
NM_001026213.1:c.1263C>A
(CYP11B1)
|
NP_001021384.1:p.Phe421Leu
|
|
XM_011516870.1:c.1699C>A
(CYP11B1)
|
XP_011515172.1:p.His567Asn
|
|
XM_011516871.1:c.1630C>A
(CYP11B1)
|
XP_011515173.1:p.His544Asn
|
|
XM_011516872.1:c.1621C>A
(CYP11B1)
|
XP_011515174.1:p.His541Asn
|
|
XM_011516873.1:c.1608C>A
(CYP11B1)
|
XP_011515175.1:p.Phe536Leu
|
|
XM_011516874.1:c.1539C>A
(CYP11B1)
|
XP_011515176.1:p.Phe513Leu
|
|
XM_011516875.1:c.1438C>A
(CYP11B1)
|
XP_011515177.1:p.His480Asn
|
|
XM_011516876.1:c.1410C>A
(CYP11B1)
|
XP_011515178.1:p.Phe470Leu
|
|
XM_011516970.1:c.214+33199G>T
(GML)
|
XP_011515272.1:n.214+33199G>T
|
|
NM_000497.4:c.1461C>A
(CYP11B1)
MANE Select
|
NP_000488.3:p.Phe487Leu
|
|