ENST00000282516.13:c.8392G>T
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Ala2798Ser
|
|
ENST00000652901.1:c.*336G>T
(NIPBL)
|
ENSP00000499536.1:n.*336G>T
|
|
ENST00000282516.12:c.8392G>T
(NIPBL)
|
ENSP00000282516.8:p.Ala2798Ser
|
|
ENST00000514335.1:n.2315G>T
(NIPBL)
|
|
|
ENST00000621733.1:c.292G>T
(NIPBL)
|
ENSP00000480694.1:p.Ala98Ser
|
|
NM_015384.4:c.*846G>T
(NIPBL)
|
NP_056199.2:n.*846G>T
|
|
NM_133433.3:c.8392G>T
(NIPBL)
|
NP_597677.2:p.Ala2798Ser
|
|
XM_005248280.2:c.*336G>T
(NIPBL)
|
XP_005248337.1:n.*336G>T
|
|
XM_005248282.3:c.7648G>T
(NIPBL)
|
XP_005248339.2:p.Ala2550Ser
|
|
XM_006714467.2:c.8245G>T
(NIPBL)
|
XP_006714530.1:p.Ala2749Ser
|
|
XM_006714468.1:c.8194G>T
(NIPBL)
|
XP_006714531.1:p.Ala2732Ser
|
|
XM_011514014.1:c.8011G>T
(NIPBL)
|
XP_011512316.1:p.Ala2671Ser
|
|
XM_005248280.3:c.*336G>T
(NIPBL)
|
XP_005248337.1:n.*336G>T
|
|
XM_005248282.5:c.7732G>T
(NIPBL)
|
XP_005248339.3:p.Ala2578Ser
|
|
XM_006714468.2:c.8194G>T
(NIPBL)
|
XP_006714531.1:p.Ala2732Ser
|
|
XM_017009329.1:c.*336G>T
(NIPBL)
|
XP_016864818.1:n.*336G>T
|
|
XM_017009330.2:c.6775G>T
(NIPBL)
|
XP_016864819.1:p.Ala2259Ser
|
|
XM_017009331.1:c.6766G>T
(NIPBL)
|
XP_016864820.1:p.Ala2256Ser
|
|
XR_925644.2:n.11813C>A
(CPLANE1)
|
|
|
NM_133433.4:c.8392G>T
(NIPBL)
MANE Select
|
NP_597677.2:p.Ala2798Ser
|
|
NM_015384.5:c.*846G>T
(NIPBL)
|
NP_056199.2:n.*846G>T
|
|