ENST00000292427.10:c.1465T>G
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Leu489Val
|
|
ENST00000292427.8:c.1465T>G
(CYP11B1)
|
ENSP00000292427.4:p.Leu489Val
|
|
ENST00000314111.4:n.1662T>G
(CYP11B1)
|
|
|
ENST00000377675.3:c.1678T>G
(CYP11B1)
|
ENSP00000366903.3:p.Leu560Val
|
|
ENST00000517471.5:c.1267T>G
(CYP11B1)
|
ENSP00000428043.1:p.Leu423Val
|
|
ENST00000519285.5:c.499T>G
(CYP11B1)
|
ENSP00000430144.1:p.Leu167Val
|
|
ENST00000522728.5:c.181+33195A>C
(GML)
|
ENSP00000430799.1:n.181+33195A>C
|
|
NM_000497.3:c.1465T>G
(CYP11B1)
|
NP_000488.3:p.Leu489Val
|
|
NM_001026213.1:c.1267T>G
(CYP11B1)
|
NP_001021384.1:p.Leu423Val
|
|
XM_011516870.1:c.1703T>G
(CYP11B1)
|
XP_011515172.1:p.Ile568Ser
|
|
XM_011516871.1:c.1634T>G
(CYP11B1)
|
XP_011515173.1:p.Ile545Ser
|
|
XM_011516872.1:c.1625T>G
(CYP11B1)
|
XP_011515174.1:p.Ile542Ser
|
|
XM_011516873.1:c.1612T>G
(CYP11B1)
|
XP_011515175.1:p.Leu538Val
|
|
XM_011516874.1:c.1543T>G
(CYP11B1)
|
XP_011515176.1:p.Leu515Val
|
|
XM_011516875.1:c.1442T>G
(CYP11B1)
|
XP_011515177.1:p.Ile481Ser
|
|
XM_011516876.1:c.1414T>G
(CYP11B1)
|
XP_011515178.1:p.Leu472Val
|
|
XM_011516970.1:c.214+33195A>C
(GML)
|
XP_011515272.1:n.214+33195A>C
|
|
NM_000497.4:c.1465T>G
(CYP11B1)
MANE Select
|
NP_000488.3:p.Leu489Val
|
|