ENST00000381884.9:c.3936T>G
(CENPJ)
MANE Select
|
ENSP00000371308.4:p.Gly1312=
|
|
ENST00000545981.6:c.*676T>G
(CENPJ)
|
ENSP00000441090.2:n.*676T>G
|
|
ENST00000381884.8:c.3936T>G
(CENPJ)
|
ENSP00000371308.4:p.Gly1312=
|
|
ENST00000545981.5:c.*677T>G
(CENPJ)
|
ENSP00000441090.2:n.*677T>G
|
|
ENST00000616936.4:c.*590T>G
(CENPJ)
|
ENSP00000477511.1:n.*590T>G
|
|
NM_018451.4:c.3936T>G
(CENPJ)
|
NP_060921.3:p.Gly1312=
|
|
NR_047594.1:n.4248T>G
(CENPJ)
|
|
|
NR_047595.1:n.4046T>G
(CENPJ)
|
|
|
XM_011535156.1:c.*10+3963A>C
(RNF17)
|
XP_011533458.1:n.*10+3963A>C
|
|
XM_011535156.2:c.*10+3963A>C
(RNF17)
|
XP_011533458.1:n.*10+3963A>C
|
|
NM_018451.5:c.3936T>G
(CENPJ)
MANE Select
|
NP_060921.3:p.Gly1312=
|
|
NR_047594.2:n.4220T>G
(CENPJ)
|
|
|
NR_047595.2:n.4018T>G
(CENPJ)
|
|
|