|
ENST00000647720.2:c.3372A>C
|
ENSP00000497673.2:p.Glu1124Asp
|
|
|
ENST00000647978.2:c.*3086A>C
|
ENSP00000497658.1:n.*3086A>C
|
|
|
ENST00000649781.2:c.3189A>C
|
ENSP00000497203.1:p.Glu1063Asp
|
|
|
ENST00000685018.2:c.3372A>C
|
ENSP00000510194.2:p.Glu1124Asp
|
|
|
ENST00000687278.2:c.3372A>C
|
ENSP00000509593.2:p.Glu1124Asp
|
|
|
ENST00000699585.1:c.3372A>C
|
ENSP00000514456.1:p.Glu1124Asp
|
|
|
ENST00000699598.1:c.3372A>C
|
ENSP00000514467.1:p.Glu1124Asp
|
|
|
ENST00000699599.1:c.3372A>C
|
ENSP00000514468.1:p.Glu1124Asp
|
|
|
ENST00000699600.1:c.3372A>C
|
ENSP00000514469.1:p.Glu1124Asp
|
|
|
ENST00000699601.1:c.*1747A>C
|
ENSP00000514470.1:n.*1747A>C
|
|
|
ENST00000699602.1:c.3368-2A>C
|
ENSP00000514471.1:n.3368-2A>C
|
|
|
ENST00000699604.1:c.*3196A>C
|
ENSP00000514472.1:n.*3196A>C
|
|
|
ENST00000699605.1:c.2946A>C
|
ENSP00000514473.1:p.Glu982Asp
|
|
|
ENST00000685018.1:c.120A>C
|
ENSP00000510194.1:p.Glu40Asp
|
|
|
ENST00000687278.1:c.963A>C
|
ENSP00000509593.1:p.Glu321Asp
|
|
|
ENST00000003084.11:c.3372A>C
MANE Select
|
ENSP00000003084.6:p.Glu1124Asp
|
|
|
ENST00000647720.1:c.1022A>C
|
|
|
|
ENST00000648260.1:c.2154A>C
|
ENSP00000497957.1:p.Glu718Asp
|
|
|
ENST00000649406.1:c.3189A>C
|
ENSP00000497965.1:p.Glu1063Asp
|
|
|
ENST00000649781.1:c.3189A>C
|
ENSP00000497203.1:p.Glu1063Asp
|
|
|
ENST00000003084.10:c.3372A>C
|
ENSP00000003084.6:p.Glu1124Asp
|
|
|
ENST00000426809.5:c.3282A>C
|
ENSP00000389119.1:p.Glu1094Asp
|
|
|
ENST00000468795.1:c.197A>C
|
|
|
|
NM_000492.3:c.3372A>C , LRG_663t1:c.3372A>C
|
NP_000483.3:p.Glu1124Asp
|
|
|
XM_011515751.1:c.3462A>C
|
XP_011514053.1:p.Glu1154Asp
|
|
|
XM_011515752.1:c.3462A>C
|
XP_011514054.1:p.Glu1154Asp
|
|
|
XM_011515753.1:c.3129A>C
|
XP_011514055.1:p.Glu1043Asp
|
|
|
XM_011515754.1:c.3129A>C
|
XP_011514056.1:p.Glu1043Asp
|
|
|
NM_000492.4:c.3372A>C
MANE Select
|
NP_000483.3:p.Glu1124Asp
|
|
