ENST00000292427.10:c.1174C>T
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Leu392Phe
|
|
ENST00000292427.8:c.1174C>T
(CYP11B1)
|
ENSP00000292427.4:p.Leu392Phe
|
|
ENST00000314111.4:n.1569C>T
(CYP11B1)
|
|
|
ENST00000377675.3:c.1387C>T
(CYP11B1)
|
ENSP00000366903.3:p.Leu463Phe
|
|
ENST00000517471.5:c.1174C>T
(CYP11B1)
|
ENSP00000428043.1:p.Leu392Phe
|
|
ENST00000519285.5:c.208C>T
(CYP11B1)
|
ENSP00000430144.1:p.Leu70Phe
|
|
ENST00000522728.5:c.181+34035G>A
(GML)
|
ENSP00000430799.1:n.181+34035G>A
|
|
NM_000497.3:c.1174C>T
(CYP11B1)
|
NP_000488.3:p.Leu392Phe
|
|
NM_001026213.1:c.1174C>T
(CYP11B1)
|
NP_001021384.1:p.Leu392Phe
|
|
XM_011516870.1:c.1321C>T
(CYP11B1)
|
XP_011515172.1:p.Leu441Phe
|
|
XM_011516871.1:c.1252C>T
(CYP11B1)
|
XP_011515173.1:p.Leu418Phe
|
|
XM_011516872.1:c.1243C>T
(CYP11B1)
|
XP_011515174.1:p.Leu415Phe
|
|
XM_011516873.1:c.1321C>T
(CYP11B1)
|
XP_011515175.1:p.Leu441Phe
|
|
XM_011516874.1:c.1252C>T
(CYP11B1)
|
XP_011515176.1:p.Leu418Phe
|
|
XM_011516875.1:c.1060C>T
(CYP11B1)
|
XP_011515177.1:p.Leu354Phe
|
|
XM_011516876.1:c.1321C>T
(CYP11B1)
|
XP_011515178.1:p.Leu441Phe
|
|
XM_011516970.1:c.214+34035G>A
(GML)
|
XP_011515272.1:n.214+34035G>A
|
|
NM_000497.4:c.1174C>T
(CYP11B1)
MANE Select
|
NP_000488.3:p.Leu392Phe
|
|