ENST00000433363.7:c.512A>T
MANE Select
|
ENSP00000406220.2:p.Glu171Val
|
|
ENST00000293800.10:c.461A>T
|
ENSP00000293800.6:p.Glu154Val
|
|
ENST00000381074.8:c.383A>T
|
ENSP00000370464.4:p.Glu128Val
|
|
ENST00000433363.6:c.512A>T
|
ENSP00000406220.2:p.Glu171Val
|
|
ENST00000572094.1:c.*262A>T
|
ENSP00000461495.1:n.*262A>T
|
|
ENST00000572352.5:c.401A>T
|
ENSP00000461622.1:p.Glu134Val
|
|
ENST00000573648.5:c.512A>T
|
ENSP00000459372.1:p.Glu171Val
|
|
ENST00000574824.5:n.1645A>T
|
|
|
ENST00000576323.1:n.542A>T
|
|
|
NM_001143838.2:c.512A>T
|
NP_001137310.1:p.Glu171Val
|
|
NM_001284509.1:c.461A>T
|
NP_001271438.1:p.Glu154Val
|
|
NM_001284510.1:c.383A>T
|
NP_001271439.1:p.Glu128Val
|
|
NM_177550.4:c.512A>T , LRG_1020t1:c.512A>T
|
NP_808218.1:p.Glu171Val
|
|
XM_006721504.2:c.401A>T
|
XP_006721567.1:p.Glu134Val
|
|
XM_011523795.1:c.512A>T
|
XP_011522097.1:p.Glu171Val
|
|
XM_011523795.3:c.512A>T
|
XP_011522097.1:p.Glu171Val
|
|
NM_001143838.3:c.512A>T
|
NP_001137310.1:p.Glu171Val
|
|
NM_001284509.2:c.461A>T
|
NP_001271438.1:p.Glu154Val
|
|
NM_001284510.2:c.383A>T
|
NP_001271439.1:p.Glu128Val
|
|
NM_177550.5:c.512A>T
MANE Select
|
NP_808218.1:p.Glu171Val
|
|