ENST00000282516.13:c.8085G>A
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Thr2695=
|
|
ENST00000652901.1:c.*29G>A
(NIPBL)
|
ENSP00000499536.1:n.*29G>A
|
|
ENST00000282516.12:c.8085G>A
(NIPBL)
|
ENSP00000282516.8:p.Thr2695=
|
|
ENST00000514335.1:n.2008G>A
(NIPBL)
|
|
|
ENST00000621733.1:c.1-16G>A
(NIPBL)
|
ENSP00000480694.1:n.1-16G>A
|
|
NM_015384.4:c.*539G>A
(NIPBL)
|
NP_056199.2:n.*539G>A
|
|
NM_133433.3:c.8085G>A
(NIPBL)
|
NP_597677.2:p.Thr2695=
|
|
XM_005248280.2:c.*29G>A
(NIPBL)
|
XP_005248337.1:n.*29G>A
|
|
XM_005248282.3:c.7341G>A
(NIPBL)
|
XP_005248339.2:p.Thr2447=
|
|
XM_006714467.2:c.7938G>A
(NIPBL)
|
XP_006714530.1:p.Thr2646=
|
|
XM_006714468.1:c.7887G>A
(NIPBL)
|
XP_006714531.1:p.Thr2629=
|
|
XM_011514014.1:c.7704G>A
(NIPBL)
|
XP_011512316.1:p.Thr2568=
|
|
XM_005248280.3:c.*29G>A
(NIPBL)
|
XP_005248337.1:n.*29G>A
|
|
XM_005248282.5:c.7425G>A
(NIPBL)
|
XP_005248339.3:p.Thr2475=
|
|
XM_006714468.2:c.7887G>A
(NIPBL)
|
XP_006714531.1:p.Thr2629=
|
|
XM_017009329.1:c.*29G>A
(NIPBL)
|
XP_016864818.1:n.*29G>A
|
|
XM_017009330.2:c.6468G>A
(NIPBL)
|
XP_016864819.1:p.Thr2156=
|
|
XM_017009331.1:c.6459G>A
(NIPBL)
|
XP_016864820.1:p.Thr2153=
|
|
XR_925644.2:n.12120C>T
(CPLANE1)
|
|
|
NM_133433.4:c.8085G>A
(NIPBL)
MANE Select
|
NP_597677.2:p.Thr2695=
|
|
NM_015384.5:c.*539G>A
(NIPBL)
|
NP_056199.2:n.*539G>A
|
|