|
ENST00000647720.2:c.3490T>G
|
ENSP00000497673.2:p.Phe1164Val
|
|
|
ENST00000647978.2:c.*3204T>G
|
ENSP00000497658.1:n.*3204T>G
|
|
|
ENST00000649781.2:c.3307T>G
|
ENSP00000497203.1:p.Phe1103Val
|
|
|
ENST00000685018.2:c.3490T>G
|
ENSP00000510194.2:p.Phe1164Val
|
|
|
ENST00000687278.2:c.*143T>G
|
ENSP00000509593.2:n.*143T>G
|
|
|
ENST00000699585.1:c.3490T>G
|
ENSP00000514456.1:p.Phe1164Val
|
|
|
ENST00000699598.1:c.3490T>G
|
ENSP00000514467.1:p.Phe1164Val
|
|
|
ENST00000699599.1:c.3490T>G
|
ENSP00000514468.1:p.Phe1164Val
|
|
|
ENST00000699600.1:c.*151T>G
|
ENSP00000514469.1:n.*151T>G
|
|
|
ENST00000699601.1:c.*1865T>G
|
ENSP00000514470.1:n.*1865T>G
|
|
|
ENST00000699602.1:c.3484T>G
|
ENSP00000514471.1:p.Phe1162Val
|
|
|
ENST00000699604.1:c.*3314T>G
|
ENSP00000514472.1:n.*3314T>G
|
|
|
ENST00000699605.1:c.3064T>G
|
ENSP00000514473.1:p.Phe1022Val
|
|
|
ENST00000685018.1:c.238T>G
|
ENSP00000510194.1:p.Phe80Val
|
|
|
ENST00000687278.1:c.1277T>G
|
ENSP00000509593.1:n.1277T>G
|
|
|
ENST00000689011.1:c.72T>G
|
|
|
|
ENST00000003084.11:c.3490T>G
MANE Select
|
ENSP00000003084.6:p.Phe1164Val
|
|
|
ENST00000647720.1:c.1140T>G
|
|
|
|
ENST00000648260.1:c.2272T>G
|
ENSP00000497957.1:p.Phe758Val
|
|
|
ENST00000649406.1:c.3307T>G
|
ENSP00000497965.1:p.Phe1103Val
|
|
|
ENST00000649781.1:c.3307T>G
|
ENSP00000497203.1:p.Phe1103Val
|
|
|
ENST00000003084.10:c.3490T>G
|
ENSP00000003084.6:p.Phe1164Val
|
|
|
ENST00000426809.5:c.3400T>G
|
ENSP00000389119.1:p.Phe1134Val
|
|
|
ENST00000468795.1:c.315T>G
|
|
|
|
NM_000492.3:c.3490T>G , LRG_663t1:c.3490T>G
|
NP_000483.3:p.Phe1164Val
|
|
|
XM_011515751.1:c.3580T>G
|
XP_011514053.1:p.Phe1194Val
|
|
|
XM_011515752.1:c.3580T>G
|
XP_011514054.1:p.Phe1194Val
|
|
|
XM_011515753.1:c.3247T>G
|
XP_011514055.1:p.Phe1083Val
|
|
|
XM_011515754.1:c.3247T>G
|
XP_011514056.1:p.Phe1083Val
|
|
|
NM_000492.4:c.3490T>G
MANE Select
|
NP_000483.3:p.Phe1164Val
|
|
