ENST00000300417.11:c.1935G>C
MANE Select
|
ENSP00000300417.6:p.Glu645Asp
|
|
ENST00000472068.2:c.*1659G>C
|
ENSP00000501555.1:n.*1659G>C
|
|
ENST00000483302.6:n.2600G>C
|
|
|
ENST00000498513.6:c.*826G>C
|
ENSP00000501637.1:n.*826G>C
|
|
ENST00000674511.1:n.1534G>C
|
|
|
ENST00000674516.1:c.*551G>C
|
ENSP00000502441.1:n.*551G>C
|
|
ENST00000674621.1:n.1861-2341G>C
|
|
|
ENST00000674771.1:c.*578G>C
|
ENSP00000502627.1:n.*578G>C
|
|
ENST00000674784.1:c.*995G>C
|
ENSP00000501837.1:n.*995G>C
|
|
ENST00000674970.1:c.*1709G>C
|
ENSP00000502493.1:n.*1709G>C
|
|
ENST00000675012.1:n.1879G>C
|
|
|
ENST00000675141.1:c.1836G>C
|
ENSP00000502420.1:p.Glu612Asp
|
|
ENST00000675198.1:n.1815G>C
|
|
|
ENST00000675213.1:c.1890G>C
|
ENSP00000502218.1:p.Glu630Asp
|
|
ENST00000675224.1:c.*1G>C
|
ENSP00000501869.1:n.*1G>C
|
|
ENST00000675253.1:c.*607G>C
|
ENSP00000502557.1:n.*607G>C
|
|
ENST00000675445.1:c.*1607G>C
|
ENSP00000502253.1:n.*1607G>C
|
|
ENST00000675448.1:c.1935G>C
|
ENSP00000502167.1:p.Glu645Asp
|
|
ENST00000675521.1:n.1845G>C
|
|
|
ENST00000675572.1:c.1836G>C
|
ENSP00000501598.1:p.Glu612Asp
|
|
ENST00000675641.1:c.*677G>C
|
ENSP00000501845.1:n.*677G>C
|
|
ENST00000675657.1:c.*548G>C
|
ENSP00000502002.1:n.*548G>C
|
|
ENST00000675662.1:n.1730G>C
|
|
|
ENST00000675789.1:c.1755G>C
|
ENSP00000501954.1:p.Glu585Asp
|
|
ENST00000675883.1:c.1854G>C
|
ENSP00000501592.1:p.Glu618Asp
|
|
ENST00000675945.1:c.*576G>C
|
ENSP00000501835.1:n.*576G>C
|
|
ENST00000676014.1:c.1878G>C
|
ENSP00000502058.1:p.Glu626Asp
|
|
ENST00000676035.1:n.1597G>C
|
|
|
ENST00000676106.1:n.1972G>C
|
|
|
ENST00000676137.1:n.1965G>C
|
|
|
ENST00000676170.1:c.2016G>C
|
ENSP00000502177.1:p.Glu672Asp
|
|
ENST00000676318.1:c.*2765G>C
|
ENSP00000502300.1:n.*2765G>C
|
|
ENST00000676336.1:c.*548G>C
|
ENSP00000502686.1:n.*548G>C
|
|
ENST00000676349.1:c.*1623G>C
|
ENSP00000502155.1:n.*1623G>C
|
|
ENST00000676399.1:n.1838G>C
|
|
|
ENST00000676409.1:n.1995G>C
|
|
|
ENST00000300417.10:c.1935G>C
|
ENSP00000300417.6:p.Glu645Asp
|
|
ENST00000323301.8:c.1935G>C
|
ENSP00000322937.4:p.Glu645Asp
|
|
ENST00000373322.1:c.1935G>C
|
ENSP00000362419.1:p.Glu645Asp
|
|
ENST00000373324.8:c.1854G>C
|
ENSP00000362421.4:p.Glu618Asp
|
|
ENST00000472068.1:n.828G>C
|
|
|
ENST00000483302.5:n.1157G>C
|
|
|
NM_001005373.3:c.1935G>C
|
NP_001005373.1:p.Glu645Asp
|
|
NM_001005374.3:c.1935G>C
|
NP_001005374.1:p.Glu645Asp
|
|
NM_001190723.2:c.1854G>C
|
NP_001177652.1:p.Glu618Asp
|
|
NM_138361.5:c.1935G>C , LRG_373t1:c.1935G>C
|
NP_612370.3:p.Glu645Asp
|
|
XM_006717316.2:c.1836G>C
|
XP_006717379.1:p.Glu612Asp
|
|
XM_006717316.4:c.1836G>C
|
XP_006717379.1:p.Glu612Asp
|
|
XM_017015283.1:c.1935G>C
|
XP_016870772.1:p.Glu645Asp
|
|
XM_017015284.2:c.1146G>C
|
XP_016870773.1:p.Glu382Asp
|
|
XR_001746415.2:n.2470G>C
|
|
|
XR_929874.3:n.2294G>C
|
|
|
NM_001190723.3:c.1854G>C
|
NP_001177652.1:p.Glu618Asp
|
|
NM_001005373.4:c.1935G>C
MANE Select
|
NP_001005373.1:p.Glu645Asp
|
|
NM_001005374.4:c.1935G>C
|
NP_001005374.1:p.Glu645Asp
|
|
NM_001384142.1:c.1935G>C
|
NP_001371071.1:p.Glu645Asp
|
|
NM_001384143.1:c.1836G>C
|
NP_001371072.1:p.Glu612Asp
|
|
NM_001384144.1:c.1146G>C
|
NP_001371073.1:p.Glu382Asp
|
|
NR_168891.1:n.2464G>C
|
|
|
NR_168892.1:n.2288G>C
|
|
|