ENST00000282516.13:c.8212C>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Gln2738Glu
|
|
ENST00000652901.1:c.*156C>G
(NIPBL)
|
ENSP00000499536.1:n.*156C>G
|
|
ENST00000282516.12:c.8212C>G
(NIPBL)
|
ENSP00000282516.8:p.Gln2738Glu
|
|
ENST00000514335.1:n.2135C>G
(NIPBL)
|
|
|
ENST00000621733.1:c.112C>G
(NIPBL)
|
ENSP00000480694.1:p.Gln38Glu
|
|
NM_015384.4:c.*666C>G
(NIPBL)
|
NP_056199.2:n.*666C>G
|
|
NM_133433.3:c.8212C>G
(NIPBL)
|
NP_597677.2:p.Gln2738Glu
|
|
XM_005248280.2:c.*156C>G
(NIPBL)
|
XP_005248337.1:n.*156C>G
|
|
XM_005248282.3:c.7468C>G
(NIPBL)
|
XP_005248339.2:p.Gln2490Glu
|
|
XM_006714467.2:c.8065C>G
(NIPBL)
|
XP_006714530.1:p.Gln2689Glu
|
|
XM_006714468.1:c.8014C>G
(NIPBL)
|
XP_006714531.1:p.Gln2672Glu
|
|
XM_011514014.1:c.7831C>G
(NIPBL)
|
XP_011512316.1:p.Gln2611Glu
|
|
XM_005248280.3:c.*156C>G
(NIPBL)
|
XP_005248337.1:n.*156C>G
|
|
XM_005248282.5:c.7552C>G
(NIPBL)
|
XP_005248339.3:p.Gln2518Glu
|
|
XM_006714468.2:c.8014C>G
(NIPBL)
|
XP_006714531.1:p.Gln2672Glu
|
|
XM_017009329.1:c.*156C>G
(NIPBL)
|
XP_016864818.1:n.*156C>G
|
|
XM_017009330.2:c.6595C>G
(NIPBL)
|
XP_016864819.1:p.Gln2199Glu
|
|
XM_017009331.1:c.6586C>G
(NIPBL)
|
XP_016864820.1:p.Gln2196Glu
|
|
XR_925644.2:n.11993G>C
(CPLANE1)
|
|
|
NM_133433.4:c.8212C>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Gln2738Glu
|
|
NM_015384.5:c.*666C>G
(NIPBL)
|
NP_056199.2:n.*666C>G
|
|