ENST00000282516.13:c.8167C>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Gln2723Glu
|
|
ENST00000652901.1:c.*111C>G
(NIPBL)
|
ENSP00000499536.1:n.*111C>G
|
|
ENST00000282516.12:c.8167C>G
(NIPBL)
|
ENSP00000282516.8:p.Gln2723Glu
|
|
ENST00000514335.1:n.2090C>G
(NIPBL)
|
|
|
ENST00000621733.1:c.67C>G
(NIPBL)
|
ENSP00000480694.1:p.Gln23Glu
|
|
NM_015384.4:c.*621C>G
(NIPBL)
|
NP_056199.2:n.*621C>G
|
|
NM_133433.3:c.8167C>G
(NIPBL)
|
NP_597677.2:p.Gln2723Glu
|
|
XM_005248280.2:c.*111C>G
(NIPBL)
|
XP_005248337.1:n.*111C>G
|
|
XM_005248282.3:c.7423C>G
(NIPBL)
|
XP_005248339.2:p.Gln2475Glu
|
|
XM_006714467.2:c.8020C>G
(NIPBL)
|
XP_006714530.1:p.Gln2674Glu
|
|
XM_006714468.1:c.7969C>G
(NIPBL)
|
XP_006714531.1:p.Gln2657Glu
|
|
XM_011514014.1:c.7786C>G
(NIPBL)
|
XP_011512316.1:p.Gln2596Glu
|
|
XM_005248280.3:c.*111C>G
(NIPBL)
|
XP_005248337.1:n.*111C>G
|
|
XM_005248282.5:c.7507C>G
(NIPBL)
|
XP_005248339.3:p.Gln2503Glu
|
|
XM_006714468.2:c.7969C>G
(NIPBL)
|
XP_006714531.1:p.Gln2657Glu
|
|
XM_017009329.1:c.*111C>G
(NIPBL)
|
XP_016864818.1:n.*111C>G
|
|
XM_017009330.2:c.6550C>G
(NIPBL)
|
XP_016864819.1:p.Gln2184Glu
|
|
XM_017009331.1:c.6541C>G
(NIPBL)
|
XP_016864820.1:p.Gln2181Glu
|
|
XR_925644.2:n.12038G>C
(CPLANE1)
|
|
|
NM_133433.4:c.8167C>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Gln2723Glu
|
|
NM_015384.5:c.*621C>G
(NIPBL)
|
NP_056199.2:n.*621C>G
|
|