ENST00000381884.9:c.3843A>T
(CENPJ)
MANE Select
|
ENSP00000371308.4:p.Ile1281=
|
|
ENST00000545981.6:c.*583A>T
(CENPJ)
|
ENSP00000441090.2:n.*583A>T
|
|
ENST00000381884.8:c.3843A>T
(CENPJ)
|
ENSP00000371308.4:p.Ile1281=
|
|
ENST00000545981.5:c.*584A>T
(CENPJ)
|
ENSP00000441090.2:n.*584A>T
|
|
ENST00000616936.4:c.*497A>T
(CENPJ)
|
ENSP00000477511.1:n.*497A>T
|
|
NM_018451.4:c.3843A>T
(CENPJ)
|
NP_060921.3:p.Ile1281=
|
|
NR_047594.1:n.4155A>T
(CENPJ)
|
|
|
NR_047595.1:n.3953A>T
(CENPJ)
|
|
|
XM_011535156.1:c.*10+4056T>A
(RNF17)
|
XP_011533458.1:n.*10+4056T>A
|
|
XM_011535156.2:c.*10+4056T>A
(RNF17)
|
XP_011533458.1:n.*10+4056T>A
|
|
NM_018451.5:c.3843A>T
(CENPJ)
MANE Select
|
NP_060921.3:p.Ile1281=
|
|
NR_047594.2:n.4127A>T
(CENPJ)
|
|
|
NR_047595.2:n.3925A>T
(CENPJ)
|
|
|