ENST00000282516.13:c.8135C>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Ala2712Gly
|
|
ENST00000652901.1:c.*79C>G
(NIPBL)
|
ENSP00000499536.1:n.*79C>G
|
|
ENST00000282516.12:c.8135C>G
(NIPBL)
|
ENSP00000282516.8:p.Ala2712Gly
|
|
ENST00000514335.1:n.2058C>G
(NIPBL)
|
|
|
ENST00000621733.1:c.35C>G
(NIPBL)
|
ENSP00000480694.1:p.Ala12Gly
|
|
NM_015384.4:c.*589C>G
(NIPBL)
|
NP_056199.2:n.*589C>G
|
|
NM_133433.3:c.8135C>G
(NIPBL)
|
NP_597677.2:p.Ala2712Gly
|
|
XM_005248280.2:c.*79C>G
(NIPBL)
|
XP_005248337.1:n.*79C>G
|
|
XM_005248282.3:c.7391C>G
(NIPBL)
|
XP_005248339.2:p.Ala2464Gly
|
|
XM_006714467.2:c.7988C>G
(NIPBL)
|
XP_006714530.1:p.Ala2663Gly
|
|
XM_006714468.1:c.7937C>G
(NIPBL)
|
XP_006714531.1:p.Ala2646Gly
|
|
XM_011514014.1:c.7754C>G
(NIPBL)
|
XP_011512316.1:p.Ala2585Gly
|
|
XM_005248280.3:c.*79C>G
(NIPBL)
|
XP_005248337.1:n.*79C>G
|
|
XM_005248282.5:c.7475C>G
(NIPBL)
|
XP_005248339.3:p.Ala2492Gly
|
|
XM_006714468.2:c.7937C>G
(NIPBL)
|
XP_006714531.1:p.Ala2646Gly
|
|
XM_017009329.1:c.*79C>G
(NIPBL)
|
XP_016864818.1:n.*79C>G
|
|
XM_017009330.2:c.6518C>G
(NIPBL)
|
XP_016864819.1:p.Ala2173Gly
|
|
XM_017009331.1:c.6509C>G
(NIPBL)
|
XP_016864820.1:p.Ala2170Gly
|
|
XR_925644.2:n.12070G>C
(CPLANE1)
|
|
|
NM_133433.4:c.8135C>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Ala2712Gly
|
|
NM_015384.5:c.*589C>G
(NIPBL)
|
NP_056199.2:n.*589C>G
|
|