ENST00000282516.13:c.8265T>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Asp2755Glu
|
|
ENST00000652901.1:c.*209T>G
(NIPBL)
|
ENSP00000499536.1:n.*209T>G
|
|
ENST00000282516.12:c.8265T>G
(NIPBL)
|
ENSP00000282516.8:p.Asp2755Glu
|
|
ENST00000514335.1:n.2188T>G
(NIPBL)
|
|
|
ENST00000621733.1:c.165T>G
(NIPBL)
|
ENSP00000480694.1:p.Asp55Glu
|
|
NM_015384.4:c.*719T>G
(NIPBL)
|
NP_056199.2:n.*719T>G
|
|
NM_133433.3:c.8265T>G
(NIPBL)
|
NP_597677.2:p.Asp2755Glu
|
|
XM_005248280.2:c.*209T>G
(NIPBL)
|
XP_005248337.1:n.*209T>G
|
|
XM_005248282.3:c.7521T>G
(NIPBL)
|
XP_005248339.2:p.Asp2507Glu
|
|
XM_006714467.2:c.8118T>G
(NIPBL)
|
XP_006714530.1:p.Asp2706Glu
|
|
XM_006714468.1:c.8067T>G
(NIPBL)
|
XP_006714531.1:p.Asp2689Glu
|
|
XM_011514014.1:c.7884T>G
(NIPBL)
|
XP_011512316.1:p.Asp2628Glu
|
|
XM_005248280.3:c.*209T>G
(NIPBL)
|
XP_005248337.1:n.*209T>G
|
|
XM_005248282.5:c.7605T>G
(NIPBL)
|
XP_005248339.3:p.Asp2535Glu
|
|
XM_006714468.2:c.8067T>G
(NIPBL)
|
XP_006714531.1:p.Asp2689Glu
|
|
XM_017009329.1:c.*209T>G
(NIPBL)
|
XP_016864818.1:n.*209T>G
|
|
XM_017009330.2:c.6648T>G
(NIPBL)
|
XP_016864819.1:p.Asp2216Glu
|
|
XM_017009331.1:c.6639T>G
(NIPBL)
|
XP_016864820.1:p.Asp2213Glu
|
|
XR_925644.2:n.11940A>C
(CPLANE1)
|
|
|
NM_133433.4:c.8265T>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Asp2755Glu
|
|
NM_015384.5:c.*719T>G
(NIPBL)
|
NP_056199.2:n.*719T>G
|
|