|
ENST00000375687.10:c.3680A>T
MANE Select
|
ENSP00000364839.4:p.Glu1227Val
|
|
|
ENST00000646985.1:c.3497A>T
|
ENSP00000495053.1:p.Glu1166Val
|
|
|
ENST00000647223.1:n.6033A>T
|
|
|
|
ENST00000651418.1:c.1869+1811A>T
|
ENSP00000499150.1:n.1869+1811A>T
|
|
|
ENST00000306058.9:c.3665A>T
|
ENSP00000305119.5:p.Glu1222Val
|
|
|
ENST00000375687.8:c.3680A>T
|
ENSP00000364839.4:p.Glu1227Val
|
|
|
ENST00000613218.4:c.3680A>T
|
ENSP00000480487.1:p.Glu1227Val
|
|
|
ENST00000620121.4:c.3680A>T
|
ENSP00000481978.1:p.Glu1227Val
|
|
|
NM_015338.5:c.3680A>T , LRG_630t1:c.3680A>T
|
NP_056153.2:p.Glu1227Val
|
|
|
XM_006723727.2:c.3677A>T
|
XP_006723790.1:p.Glu1226Val
|
|
|
XM_006723728.2:c.3650A>T
|
XP_006723791.1:p.Glu1217Val
|
|
|
XM_006723730.2:c.3596A>T
|
XP_006723793.1:p.Glu1199Val
|
|
|
XM_006723732.2:c.3497A>T
|
XP_006723795.1:p.Glu1166Val
|
|
|
XM_006723733.1:c.2996A>T
|
XP_006723796.1:p.Glu999Val
|
|
|
XM_011528647.1:c.3944A>T
|
XP_011526949.1:p.Glu1315Val
|
|
|
XM_011528648.1:c.3941A>T
|
XP_011526950.1:p.Glu1314Val
|
|
|
XM_011528649.1:c.3860A>T
|
XP_011526951.1:p.Glu1287Val
|
|
|
XM_011528650.1:c.3791A>T
|
XP_011526952.1:p.Glu1264Val
|
|
|
XM_011528651.1:c.3659A>T
|
XP_011526953.1:p.Glu1220Val
|
|
|
XM_011528652.1:c.3596A>T
|
XP_011526954.1:p.Glu1199Val
|
|
|
NM_001363734.1:c.3497A>T
|
NP_001350663.1:p.Glu1166Val
|
|
|
XM_006723727.3:c.3677A>T
|
XP_006723790.1:p.Glu1226Val
|
|
|
XM_006723728.3:c.3650A>T
|
XP_006723791.1:p.Glu1217Val
|
|
|
XM_006723730.4:c.3596A>T
|
XP_006723793.1:p.Glu1199Val
|
|
|
XM_011528648.3:c.3941A>T
|
XP_011526950.1:p.Glu1314Val
|
|
|
XM_011528652.2:c.3596A>T
|
XP_011526954.1:p.Glu1199Val
|
|
|
XM_017027704.1:c.3596A>T
|
XP_016883193.1:p.Glu1199Val
|
|
|
XM_017027705.1:c.3596A>T
|
XP_016883194.1:p.Glu1199Val
|
|
|
XM_017027706.1:c.3527A>T
|
XP_016883195.1:p.Glu1176Val
|
|
|
NM_015338.6:c.3680A>T
MANE Select
|
NP_056153.2:p.Glu1227Val
|
|
