ENST00000282516.13:c.8273A>C
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Lys2758Thr
|
|
ENST00000652901.1:c.*217A>C
(NIPBL)
|
ENSP00000499536.1:n.*217A>C
|
|
ENST00000282516.12:c.8273A>C
(NIPBL)
|
ENSP00000282516.8:p.Lys2758Thr
|
|
ENST00000514335.1:n.2196A>C
(NIPBL)
|
|
|
ENST00000621733.1:c.173A>C
(NIPBL)
|
ENSP00000480694.1:p.Lys58Thr
|
|
NM_015384.4:c.*727A>C
(NIPBL)
|
NP_056199.2:n.*727A>C
|
|
NM_133433.3:c.8273A>C
(NIPBL)
|
NP_597677.2:p.Lys2758Thr
|
|
XM_005248280.2:c.*217A>C
(NIPBL)
|
XP_005248337.1:n.*217A>C
|
|
XM_005248282.3:c.7529A>C
(NIPBL)
|
XP_005248339.2:p.Lys2510Thr
|
|
XM_006714467.2:c.8126A>C
(NIPBL)
|
XP_006714530.1:p.Lys2709Thr
|
|
XM_006714468.1:c.8075A>C
(NIPBL)
|
XP_006714531.1:p.Lys2692Thr
|
|
XM_011514014.1:c.7892A>C
(NIPBL)
|
XP_011512316.1:p.Lys2631Thr
|
|
XM_005248280.3:c.*217A>C
(NIPBL)
|
XP_005248337.1:n.*217A>C
|
|
XM_005248282.5:c.7613A>C
(NIPBL)
|
XP_005248339.3:p.Lys2538Thr
|
|
XM_006714468.2:c.8075A>C
(NIPBL)
|
XP_006714531.1:p.Lys2692Thr
|
|
XM_017009329.1:c.*217A>C
(NIPBL)
|
XP_016864818.1:n.*217A>C
|
|
XM_017009330.2:c.6656A>C
(NIPBL)
|
XP_016864819.1:p.Lys2219Thr
|
|
XM_017009331.1:c.6647A>C
(NIPBL)
|
XP_016864820.1:p.Lys2216Thr
|
|
XR_925644.2:n.11932T>G
(CPLANE1)
|
|
|
NM_133433.4:c.8273A>C
(NIPBL)
MANE Select
|
NP_597677.2:p.Lys2758Thr
|
|
NM_015384.5:c.*727A>C
(NIPBL)
|
NP_056199.2:n.*727A>C
|
|