ENST00000381884.9:c.*326A>C
(CENPJ)
MANE Select
|
ENSP00000371308.4:n.*326A>C
|
|
ENST00000616936.4:c.*997A>C
(CENPJ)
|
ENSP00000477511.1:n.*997A>C
|
|
NM_018451.4:c.*326A>C
(CENPJ)
|
NP_060921.3:n.*326A>C
|
|
NR_047594.1:n.4655A>C
(CENPJ)
|
|
|
NR_047595.1:n.4453A>C
(CENPJ)
|
|
|
XM_011535156.1:c.*10+3556T>G
(RNF17)
|
XP_011533458.1:n.*10+3556T>G
|
|
XM_011535156.2:c.*10+3556T>G
(RNF17)
|
XP_011533458.1:n.*10+3556T>G
|
|
NM_018451.5:c.*326A>C
(CENPJ)
MANE Select
|
NP_060921.3:n.*326A>C
|
|
NR_047594.2:n.4627A>C
(CENPJ)
|
|
|
NR_047595.2:n.4425A>C
(CENPJ)
|
|
|