ENST00000282516.13:c.8154C>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Tyr2718Ter
|
|
ENST00000652901.1:c.*98C>G
(NIPBL)
|
ENSP00000499536.1:n.*98C>G
|
|
ENST00000282516.12:c.8154C>G
(NIPBL)
|
ENSP00000282516.8:p.Tyr2718Ter
|
|
ENST00000514335.1:n.2077C>G
(NIPBL)
|
|
|
ENST00000621733.1:c.54C>G
(NIPBL)
|
ENSP00000480694.1:p.Tyr18Ter
|
|
NM_015384.4:c.*608C>G
(NIPBL)
|
NP_056199.2:n.*608C>G
|
|
NM_133433.3:c.8154C>G
(NIPBL)
|
NP_597677.2:p.Tyr2718Ter
|
|
XM_005248280.2:c.*98C>G
(NIPBL)
|
XP_005248337.1:n.*98C>G
|
|
XM_005248282.3:c.7410C>G
(NIPBL)
|
XP_005248339.2:p.Tyr2470Ter
|
|
XM_006714467.2:c.8007C>G
(NIPBL)
|
XP_006714530.1:p.Tyr2669Ter
|
|
XM_006714468.1:c.7956C>G
(NIPBL)
|
XP_006714531.1:p.Tyr2652Ter
|
|
XM_011514014.1:c.7773C>G
(NIPBL)
|
XP_011512316.1:p.Tyr2591Ter
|
|
XM_005248280.3:c.*98C>G
(NIPBL)
|
XP_005248337.1:n.*98C>G
|
|
XM_005248282.5:c.7494C>G
(NIPBL)
|
XP_005248339.3:p.Tyr2498Ter
|
|
XM_006714468.2:c.7956C>G
(NIPBL)
|
XP_006714531.1:p.Tyr2652Ter
|
|
XM_017009329.1:c.*98C>G
(NIPBL)
|
XP_016864818.1:n.*98C>G
|
|
XM_017009330.2:c.6537C>G
(NIPBL)
|
XP_016864819.1:p.Tyr2179Ter
|
|
XM_017009331.1:c.6528C>G
(NIPBL)
|
XP_016864820.1:p.Tyr2176Ter
|
|
XR_925644.2:n.12051G>C
(CPLANE1)
|
|
|
NM_133433.4:c.8154C>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Tyr2718Ter
|
|
NM_015384.5:c.*608C>G
(NIPBL)
|
NP_056199.2:n.*608C>G
|
|