ENST00000282516.13:c.8054T>G
(NIPBL)
MANE Select
|
ENSP00000282516.8:p.Leu2685Trp
|
|
ENST00000652901.1:c.7948T>G
(NIPBL)
|
ENSP00000499536.1:p.Ter2650Gly
|
|
ENST00000282516.12:c.8054T>G
(NIPBL)
|
ENSP00000282516.8:p.Leu2685Trp
|
|
ENST00000514335.1:n.1977T>G
(NIPBL)
|
|
|
ENST00000621733.1:c.1-47T>G
(NIPBL)
|
ENSP00000480694.1:n.1-47T>G
|
|
NM_015384.4:c.*508T>G
(NIPBL)
|
NP_056199.2:n.*508T>G
|
|
NM_133433.3:c.8054T>G
(NIPBL)
|
NP_597677.2:p.Leu2685Trp
|
|
XM_005248280.2:c.8095T>G
(NIPBL)
|
XP_005248337.1:p.Ter2699Gly
|
|
XM_005248282.3:c.7310T>G
(NIPBL)
|
XP_005248339.2:p.Leu2437Trp
|
|
XM_006714467.2:c.7907T>G
(NIPBL)
|
XP_006714530.1:p.Leu2636Trp
|
|
XM_006714468.1:c.7856T>G
(NIPBL)
|
XP_006714531.1:p.Leu2619Trp
|
|
XM_011514014.1:c.7673T>G
(NIPBL)
|
XP_011512316.1:p.Leu2558Trp
|
|
XM_005248280.3:c.8095T>G
(NIPBL)
|
XP_005248337.1:p.Ter2699Gly
|
|
XM_005248282.5:c.7394T>G
(NIPBL)
|
XP_005248339.3:p.Leu2465Trp
|
|
XM_006714468.2:c.7856T>G
(NIPBL)
|
XP_006714531.1:p.Leu2619Trp
|
|
XM_017009329.1:c.7948T>G
(NIPBL)
|
XP_016864818.1:p.Ter2650Gly
|
|
XM_017009330.2:c.6437T>G
(NIPBL)
|
XP_016864819.1:p.Leu2146Trp
|
|
XM_017009331.1:c.6428T>G
(NIPBL)
|
XP_016864820.1:p.Leu2143Trp
|
|
XR_925644.2:n.12151A>C
(CPLANE1)
|
|
|
NM_133433.4:c.8054T>G
(NIPBL)
MANE Select
|
NP_597677.2:p.Leu2685Trp
|
|
NM_015384.5:c.*508T>G
(NIPBL)
|
NP_056199.2:n.*508T>G
|
|