ENST00000381884.9:c.3928G>A
(CENPJ)
MANE Select
|
ENSP00000371308.4:p.Ala1310Thr
|
|
ENST00000545981.6:c.*668G>A
(CENPJ)
|
ENSP00000441090.2:n.*668G>A
|
|
ENST00000381884.8:c.3928G>A
(CENPJ)
|
ENSP00000371308.4:p.Ala1310Thr
|
|
ENST00000545981.5:c.*669G>A
(CENPJ)
|
ENSP00000441090.2:n.*669G>A
|
|
ENST00000616936.4:c.*582G>A
(CENPJ)
|
ENSP00000477511.1:n.*582G>A
|
|
NM_018451.4:c.3928G>A
(CENPJ)
|
NP_060921.3:p.Ala1310Thr
|
|
NR_047594.1:n.4240G>A
(CENPJ)
|
|
|
NR_047595.1:n.4038G>A
(CENPJ)
|
|
|
XM_011535156.1:c.*10+3971C>T
(RNF17)
|
XP_011533458.1:n.*10+3971C>T
|
|
XM_011535156.2:c.*10+3971C>T
(RNF17)
|
XP_011533458.1:n.*10+3971C>T
|
|
NM_018451.5:c.3928G>A
(CENPJ)
MANE Select
|
NP_060921.3:p.Ala1310Thr
|
|
NR_047594.2:n.4212G>A
(CENPJ)
|
|
|
NR_047595.2:n.4010G>A
(CENPJ)
|
|
|