ENST00000381884.9:c.*315G>T
(CENPJ)
MANE Select
|
ENSP00000371308.4:n.*315G>T
|
|
ENST00000616936.4:c.*986G>T
(CENPJ)
|
ENSP00000477511.1:n.*986G>T
|
|
NM_018451.4:c.*315G>T
(CENPJ)
|
NP_060921.3:n.*315G>T
|
|
NR_047594.1:n.4644G>T
(CENPJ)
|
|
|
NR_047595.1:n.4442G>T
(CENPJ)
|
|
|
XM_011535156.1:c.*10+3567C>A
(RNF17)
|
XP_011533458.1:n.*10+3567C>A
|
|
XM_011535156.2:c.*10+3567C>A
(RNF17)
|
XP_011533458.1:n.*10+3567C>A
|
|
NM_018451.5:c.*315G>T
(CENPJ)
MANE Select
|
NP_060921.3:n.*315G>T
|
|
NR_047594.2:n.4616G>T
(CENPJ)
|
|
|
NR_047595.2:n.4414G>T
(CENPJ)
|
|
|