|
ENST00000647720.2:c.3311A>T
|
ENSP00000497673.2:p.Glu1104Val
|
|
|
ENST00000647978.2:c.*3025A>T
|
ENSP00000497658.1:n.*3025A>T
|
|
|
ENST00000649781.2:c.3128A>T
|
ENSP00000497203.1:p.Glu1043Val
|
|
|
ENST00000685018.2:c.3311A>T
|
ENSP00000510194.2:p.Glu1104Val
|
|
|
ENST00000687278.2:c.3311A>T
|
ENSP00000509593.2:p.Glu1104Val
|
|
|
ENST00000699585.1:c.3311A>T
|
ENSP00000514456.1:p.Glu1104Val
|
|
|
ENST00000699598.1:c.3311A>T
|
ENSP00000514467.1:p.Glu1104Val
|
|
|
ENST00000699599.1:c.3311A>T
|
ENSP00000514468.1:p.Glu1104Val
|
|
|
ENST00000699600.1:c.3311A>T
|
ENSP00000514469.1:p.Glu1104Val
|
|
|
ENST00000699601.1:c.*1611A>T
|
ENSP00000514470.1:n.*1611A>T
|
|
|
ENST00000699602.1:c.3311A>T
|
ENSP00000514471.1:p.Glu1104Val
|
|
|
ENST00000699604.1:c.*3135A>T
|
ENSP00000514472.1:n.*3135A>T
|
|
|
ENST00000699605.1:c.2885A>T
|
ENSP00000514473.1:p.Glu962Val
|
|
|
ENST00000685018.1:c.59A>T
|
ENSP00000510194.1:p.Glu20Val
|
|
|
ENST00000687278.1:c.902A>T
|
ENSP00000509593.1:p.Glu301Val
|
|
|
ENST00000003084.11:c.3311A>T
MANE Select
|
ENSP00000003084.6:p.Glu1104Val
|
|
|
ENST00000647720.1:c.961A>T
|
|
|
|
ENST00000648260.1:c.2093A>T
|
ENSP00000497957.1:p.Glu698Val
|
|
|
ENST00000649406.1:c.3128A>T
|
ENSP00000497965.1:p.Glu1043Val
|
|
|
ENST00000649781.1:c.3128A>T
|
ENSP00000497203.1:p.Glu1043Val
|
|
|
ENST00000003084.10:c.3311A>T
|
ENSP00000003084.6:p.Glu1104Val
|
|
|
ENST00000426809.5:c.3221A>T
|
ENSP00000389119.1:p.Glu1074Val
|
|
|
ENST00000468795.1:c.136A>T
|
|
|
|
NM_000492.3:c.3311A>T , LRG_663t1:c.3311A>T
|
NP_000483.3:p.Glu1104Val
|
|
|
XM_011515751.1:c.3401A>T
|
XP_011514053.1:p.Glu1134Val
|
|
|
XM_011515752.1:c.3401A>T
|
XP_011514054.1:p.Glu1134Val
|
|
|
XM_011515753.1:c.3068A>T
|
XP_011514055.1:p.Glu1023Val
|
|
|
XM_011515754.1:c.3068A>T
|
XP_011514056.1:p.Glu1023Val
|
|
|
NM_000492.4:c.3311A>T
MANE Select
|
NP_000483.3:p.Glu1104Val
|
|
