|
ENST00000287152.12:c.2153A>T
MANE Select
|
ENSP00000287152.7:p.Glu718Val
|
|
|
ENST00000229913.9:c.506A>T
|
ENSP00000229913.5:p.Glu169Val
|
|
|
ENST00000287152.11:c.2153A>T
|
ENSP00000287152.7:p.Glu718Val
|
|
|
ENST00000394362.5:c.506A>T
|
ENSP00000377889.1:p.Glu169Val
|
|
|
ENST00000458470.5:c.1828A>T
|
|
|
|
ENST00000538893.5:c.506A>T
|
ENSP00000441435.2:p.Glu169Val
|
|
|
NM_001289020.1:c.2102A>T
|
NP_001275949.1:p.Glu701Val
|
|
|
NM_001289021.1:c.1985A>T
|
NP_001275950.1:p.Glu662Val
|
|
|
NM_001289024.1:c.506A>T
|
NP_001275953.1:p.Glu169Val
|
|
|
NM_145027.4:c.2153A>T
|
NP_659464.3:p.Glu718Val
|
|
|
XM_005248904.3:c.2153A>T
|
XP_005248961.1:p.Glu718Val
|
|
|
XM_011514357.1:c.2153A>T
|
XP_011512659.1:p.Glu718Val
|
|
|
XM_011514358.1:c.2153A>T
|
XP_011512660.1:p.Glu718Val
|
|
|
XM_011514359.1:c.2153A>T
|
XP_011512661.1:p.Glu718Val
|
|
|
XM_011514360.1:c.1526A>T
|
XP_011512662.1:p.Glu509Val
|
|
|
NM_001289020.2:c.2102A>T
|
NP_001275949.1:p.Glu701Val
|
|
|
NM_001289021.2:c.1985A>T
|
NP_001275950.1:p.Glu662Val
|
|
|
NM_001289024.2:c.506A>T
|
NP_001275953.1:p.Glu169Val
|
|
|
NM_001351566.1:c.506A>T
|
NP_001338495.1:p.Glu169Val
|
|
|
NM_145027.5:c.2153A>T
|
NP_659464.3:p.Glu718Val
|
|
|
XM_005248904.4:c.2153A>T
|
XP_005248961.1:p.Glu718Val
|
|
|
XM_011514357.3:c.2153A>T
|
XP_011512659.1:p.Glu718Val
|
|
|
XM_011514358.3:c.2153A>T
|
XP_011512660.1:p.Glu718Val
|
|
|
XM_011514359.3:c.2153A>T
|
XP_011512661.1:p.Glu718Val
|
|
|
XM_017010427.1:c.1844A>T
|
XP_016865916.1:p.Glu615Val
|
|
|
XM_017010428.1:c.1508A>T
|
XP_016865917.1:p.Glu503Val
|
|
|
XR_001744111.1:n.75+5356T>A
|
|
|
|
NM_145027.6:c.2153A>T
MANE Select
|
NP_659464.3:p.Glu718Val
|
|
|
NM_001289020.3:c.2102A>T
|
NP_001275949.1:p.Glu701Val
|
|
|
NM_001289021.3:c.1985A>T
|
NP_001275950.1:p.Glu662Val
|
|
|
NM_001289024.3:c.506A>T
|
NP_001275953.1:p.Glu169Val
|
|
|
NM_001351566.2:c.506A>T
|
NP_001338495.1:p.Glu169Val
|
|
