ENST00000287936.9:c.2398A=
(HMGCR)
MANE Select
|
ENSP00000287936.4:p.Ile800=
|
|
ENST00000644912.1:c.1670-2485T=
(CERT1)
|
ENSP00000495172.1:n.1670-2485T=
|
|
ENST00000646172.1:c.1203-2485T=
(CERT1)
|
ENSP00000494969.1:n.1203-2485T=
|
|
ENST00000679456.1:n.3235A=
(HMGCR)
|
|
|
ENST00000680160.1:c.2398A=
(HMGCR)
|
ENSP00000505315.1:p.Ile800=
|
|
ENST00000680940.1:c.2398A=
(HMGCR)
|
ENSP00000505561.1:p.Ile800=
|
|
ENST00000681271.1:c.2398A=
(HMGCR)
|
ENSP00000505805.1:p.Ile800=
|
|
ENST00000681410.1:c.2398A=
(HMGCR)
|
ENSP00000506232.1:p.Ile800=
|
|
ENST00000681567.1:c.*2947A=
(HMGCR)
|
ENSP00000506708.1:n.*2947A=
|
|
ENST00000287936.8:c.2398A=
(HMGCR)
|
ENSP00000287936.4:p.Ile800=
|
|
ENST00000343975.9:c.2239A=
(HMGCR)
|
ENSP00000340816.5:p.Ile747=
|
|
ENST00000509085.5:c.287+187A=
(HMGCR)
|
|
|
ENST00000511206.5:c.2398A=
(HMGCR)
|
ENSP00000426745.1:p.Ile800=
|
|
ENST00000511986.1:c.139-488A=
(HMGCR)
|
ENSP00000420871.1:n.139-488A=
|
|
ENST00000514315.2:n.339A=
(HMGCR)
|
|
|
NM_000859.2:c.2398A=
(HMGCR)
|
NP_000850.1:p.Ile800=
|
|
NM_001130996.1:c.2239A=
(HMGCR)
|
NP_001124468.1:p.Ile747=
|
|
XM_011543357.1:c.2458A=
(HMGCR)
|
XP_011541659.1:p.Ile820=
|
|
XM_011543358.1:c.2398A=
(HMGCR)
|
XP_011541660.1:p.Ile800=
|
|
XM_011543359.1:c.2299A=
(HMGCR)
|
XP_011541661.1:p.Ile767=
|
|
NM_001364187.1:c.2398A=
(HMGCR)
|
NP_001351116.1:p.Ile800=
|
|
NM_000859.3:c.2398A=
(HMGCR)
MANE Select
|
NP_000850.1:p.Ile800=
|
|
NM_001130996.2:c.2239A=
(HMGCR)
|
NP_001124468.1:p.Ile747=
|
|