ENST00000300417.11:c.2002C>G
MANE Select
|
ENSP00000300417.6:p.Leu668Val
|
|
ENST00000472068.2:c.*1726C>G
|
ENSP00000501555.1:n.*1726C>G
|
|
ENST00000483302.6:n.2667C>G
|
|
|
ENST00000498513.6:c.*893C>G
|
ENSP00000501637.1:n.*893C>G
|
|
ENST00000674511.1:n.1601C>G
|
|
|
ENST00000674516.1:c.*618C>G
|
ENSP00000502441.1:n.*618C>G
|
|
ENST00000674621.1:n.1861-2274C>G
|
|
|
ENST00000674771.1:c.*645C>G
|
ENSP00000502627.1:n.*645C>G
|
|
ENST00000674784.1:c.*1062C>G
|
ENSP00000501837.1:n.*1062C>G
|
|
ENST00000674970.1:c.*1776C>G
|
ENSP00000502493.1:n.*1776C>G
|
|
ENST00000675012.1:n.1946C>G
|
|
|
ENST00000675141.1:c.1903C>G
|
ENSP00000502420.1:p.Leu635Val
|
|
ENST00000675198.1:n.1882C>G
|
|
|
ENST00000675213.1:c.1957C>G
|
ENSP00000502218.1:p.Leu653Val
|
|
ENST00000675224.1:c.*68C>G
|
ENSP00000501869.1:n.*68C>G
|
|
ENST00000675253.1:c.*674C>G
|
ENSP00000502557.1:n.*674C>G
|
|
ENST00000675445.1:c.*1674C>G
|
ENSP00000502253.1:n.*1674C>G
|
|
ENST00000675448.1:c.2002C>G
|
ENSP00000502167.1:p.Leu668Val
|
|
ENST00000675521.1:n.1912C>G
|
|
|
ENST00000675572.1:c.1903C>G
|
ENSP00000501598.1:p.Leu635Val
|
|
ENST00000675641.1:c.*744C>G
|
ENSP00000501845.1:n.*744C>G
|
|
ENST00000675657.1:c.*615C>G
|
ENSP00000502002.1:n.*615C>G
|
|
ENST00000675662.1:n.1797C>G
|
|
|
ENST00000675789.1:c.1822C>G
|
ENSP00000501954.1:p.Leu608Val
|
|
ENST00000675883.1:c.1921C>G
|
ENSP00000501592.1:p.Leu641Val
|
|
ENST00000675945.1:c.*643C>G
|
ENSP00000501835.1:n.*643C>G
|
|
ENST00000676014.1:c.1945C>G
|
ENSP00000502058.1:p.Leu649Val
|
|
ENST00000676035.1:n.1664C>G
|
|
|
ENST00000676106.1:n.2039C>G
|
|
|
ENST00000676137.1:n.2032C>G
|
|
|
ENST00000676170.1:c.2083C>G
|
ENSP00000502177.1:p.Leu695Val
|
|
ENST00000676318.1:c.*2832C>G
|
ENSP00000502300.1:n.*2832C>G
|
|
ENST00000676336.1:c.*615C>G
|
ENSP00000502686.1:n.*615C>G
|
|
ENST00000676349.1:c.*1690C>G
|
ENSP00000502155.1:n.*1690C>G
|
|
ENST00000676399.1:n.1905C>G
|
|
|
ENST00000676409.1:n.2062C>G
|
|
|
ENST00000300417.10:c.2002C>G
|
ENSP00000300417.6:p.Leu668Val
|
|
ENST00000323301.8:c.2002C>G
|
ENSP00000322937.4:p.Leu668Val
|
|
ENST00000373322.1:c.2002C>G
|
ENSP00000362419.1:p.Leu668Val
|
|
ENST00000373324.8:c.1921C>G
|
ENSP00000362421.4:p.Leu641Val
|
|
ENST00000483302.5:n.1224C>G
|
|
|
NM_001005373.3:c.2002C>G
|
NP_001005373.1:p.Leu668Val
|
|
NM_001005374.3:c.2002C>G
|
NP_001005374.1:p.Leu668Val
|
|
NM_001190723.2:c.1921C>G
|
NP_001177652.1:p.Leu641Val
|
|
NM_138361.5:c.2002C>G , LRG_373t1:c.2002C>G
|
NP_612370.3:p.Leu668Val
|
|
XM_006717316.2:c.1903C>G
|
XP_006717379.1:p.Leu635Val
|
|
XM_006717316.4:c.1903C>G
|
XP_006717379.1:p.Leu635Val
|
|
XM_017015283.1:c.2002C>G
|
XP_016870772.1:p.Leu668Val
|
|
XM_017015284.2:c.1213C>G
|
XP_016870773.1:p.Leu405Val
|
|
XR_001746415.2:n.2537C>G
|
|
|
XR_929874.3:n.2361C>G
|
|
|
NM_001190723.3:c.1921C>G
|
NP_001177652.1:p.Leu641Val
|
|
NM_001005373.4:c.2002C>G
MANE Select
|
NP_001005373.1:p.Leu668Val
|
|
NM_001005374.4:c.2002C>G
|
NP_001005374.1:p.Leu668Val
|
|
NM_001384142.1:c.2002C>G
|
NP_001371071.1:p.Leu668Val
|
|
NM_001384143.1:c.1903C>G
|
NP_001371072.1:p.Leu635Val
|
|
NM_001384144.1:c.1213C>G
|
NP_001371073.1:p.Leu405Val
|
|
NR_168891.1:n.2531C>G
|
|
|
NR_168892.1:n.2355C>G
|
|
|