|
ENST00000287936.9:c.2457+198A>T
(HMGCR)
MANE Select
|
ENSP00000287936.4:n.2457+198A>T
|
|
|
ENST00000644912.1:c.1670-2742T>A
(CERT1)
|
ENSP00000495172.1:n.1670-2742T>A
|
|
|
ENST00000646172.1:c.1203-2742T>A
(CERT1)
|
ENSP00000494969.1:n.1203-2742T>A
|
|
|
ENST00000679456.1:n.3294+198A>T
(HMGCR)
|
|
|
|
ENST00000680160.1:c.2413-231A>T
(HMGCR)
|
ENSP00000505315.1:n.2413-231A>T
|
|
|
ENST00000680940.1:c.2457+198A>T
(HMGCR)
|
ENSP00000505561.1:n.2457+198A>T
|
|
|
ENST00000681271.1:c.2457+198A>T
(HMGCR)
|
ENSP00000505805.1:n.2457+198A>T
|
|
|
ENST00000681410.1:c.2457+198A>T
(HMGCR)
|
ENSP00000506232.1:n.2457+198A>T
|
|
|
ENST00000681567.1:c.*3006+198A>T
(HMGCR)
|
ENSP00000506708.1:n.*3006+198A>T
|
|
|
ENST00000287936.8:c.2457+198A>T
(HMGCR)
|
ENSP00000287936.4:n.2457+198A>T
|
|
|
ENST00000343975.9:c.2298+198A>T
(HMGCR)
|
ENSP00000340816.5:n.2298+198A>T
|
|
|
ENST00000509085.5:c.288-231A>T
(HMGCR)
|
|
|
|
ENST00000511206.5:c.2457+198A>T
(HMGCR)
|
ENSP00000426745.1:n.2457+198A>T
|
|
|
ENST00000511986.1:c.139-231A>T
(HMGCR)
|
ENSP00000420871.1:n.139-231A>T
|
|
|
ENST00000514315.2:n.596A>T
(HMGCR)
|
|
|
|
NM_000859.2:c.2457+198A>T
(HMGCR)
|
NP_000850.1:n.2457+198A>T
|
|
|
NM_001130996.1:c.2298+198A>T
(HMGCR)
|
NP_001124468.1:n.2298+198A>T
|
|
|
XM_011543357.1:c.2517+198A>T
(HMGCR)
|
XP_011541659.1:n.2517+198A>T
|
|
|
XM_011543358.1:c.2457+198A>T
(HMGCR)
|
XP_011541660.1:n.2457+198A>T
|
|
|
XM_011543359.1:c.2358+198A>T
(HMGCR)
|
XP_011541661.1:n.2358+198A>T
|
|
|
NM_001364187.1:c.2457+198A>T
(HMGCR)
|
NP_001351116.1:n.2457+198A>T
|
|
|
NM_000859.3:c.2457+198A>T
(HMGCR)
MANE Select
|
NP_000850.1:n.2457+198A>T
|
|
|
NM_001130996.2:c.2298+198A>T
(HMGCR)
|
NP_001124468.1:n.2298+198A>T
|
|
