ENST00000282516.13:c.8222C>T
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Ala2741Val
|
|
ENST00000652901.1:c.*166C>T
(NIPBL)
|
ENSP00000499536.1:n.*166C>T
|
|
ENST00000282516.12:c.8222C>T
(NIPBL)
|
ENSP00000282516.8:p.Ala2741Val
|
|
ENST00000514335.1:n.2145C>T
(NIPBL)
|
|
|
ENST00000621733.1:c.122C>T
(NIPBL)
|
ENSP00000480694.1:p.Ala41Val
|
|
NM_015384.4:c.*676C>T
(NIPBL)
|
NP_056199.2:n.*676C>T
|
|
NM_133433.3:c.8222C>T
(NIPBL)
|
NP_597677.2:p.Ala2741Val
|
|
XM_005248280.2:c.*166C>T
(NIPBL)
|
XP_005248337.1:n.*166C>T
|
|
XM_005248282.3:c.7478C>T
(NIPBL)
|
XP_005248339.2:p.Ala2493Val
|
|
XM_006714467.2:c.8075C>T
(NIPBL)
|
XP_006714530.1:p.Ala2692Val
|
|
XM_006714468.1:c.8024C>T
(NIPBL)
|
XP_006714531.1:p.Ala2675Val
|
|
XM_011514014.1:c.7841C>T
(NIPBL)
|
XP_011512316.1:p.Ala2614Val
|
|
XM_005248280.3:c.*166C>T
(NIPBL)
|
XP_005248337.1:n.*166C>T
|
|
XM_005248282.5:c.7562C>T
(NIPBL)
|
XP_005248339.3:p.Ala2521Val
|
|
XM_006714468.2:c.8024C>T
(NIPBL)
|
XP_006714531.1:p.Ala2675Val
|
|
XM_017009329.1:c.*166C>T
(NIPBL)
|
XP_016864818.1:n.*166C>T
|
|
XM_017009330.2:c.6605C>T
(NIPBL)
|
XP_016864819.1:p.Ala2202Val
|
|
XM_017009331.1:c.6596C>T
(NIPBL)
|
XP_016864820.1:p.Ala2199Val
|
|
XR_925644.2:n.11983G>A
(CPLANE1)
|
|
|
NM_133433.4:c.8222C>T
(NIPBL)
MANE Select
|
NP_597677.2:p.Ala2741Val
|
|
NM_015384.5:c.*676C>T
(NIPBL)
|
NP_056199.2:n.*676C>T
|
|