|
ENST00000647720.2:c.3312A>T
|
ENSP00000497673.2:p.Glu1104Asp
|
|
|
ENST00000647978.2:c.*3026A>T
|
ENSP00000497658.1:n.*3026A>T
|
|
|
ENST00000649781.2:c.3129A>T
|
ENSP00000497203.1:p.Glu1043Asp
|
|
|
ENST00000685018.2:c.3312A>T
|
ENSP00000510194.2:p.Glu1104Asp
|
|
|
ENST00000687278.2:c.3312A>T
|
ENSP00000509593.2:p.Glu1104Asp
|
|
|
ENST00000699585.1:c.3312A>T
|
ENSP00000514456.1:p.Glu1104Asp
|
|
|
ENST00000699598.1:c.3312A>T
|
ENSP00000514467.1:p.Glu1104Asp
|
|
|
ENST00000699599.1:c.3312A>T
|
ENSP00000514468.1:p.Glu1104Asp
|
|
|
ENST00000699600.1:c.3312A>T
|
ENSP00000514469.1:p.Glu1104Asp
|
|
|
ENST00000699601.1:c.*1612A>T
|
ENSP00000514470.1:n.*1612A>T
|
|
|
ENST00000699602.1:c.3312A>T
|
ENSP00000514471.1:p.Glu1104Asp
|
|
|
ENST00000699604.1:c.*3136A>T
|
ENSP00000514472.1:n.*3136A>T
|
|
|
ENST00000699605.1:c.2886A>T
|
ENSP00000514473.1:p.Glu962Asp
|
|
|
ENST00000685018.1:c.60A>T
|
ENSP00000510194.1:p.Glu20Asp
|
|
|
ENST00000687278.1:c.903A>T
|
ENSP00000509593.1:p.Glu301Asp
|
|
|
ENST00000003084.11:c.3312A>T
MANE Select
|
ENSP00000003084.6:p.Glu1104Asp
|
|
|
ENST00000647720.1:c.962A>T
|
|
|
|
ENST00000648260.1:c.2094A>T
|
ENSP00000497957.1:p.Glu698Asp
|
|
|
ENST00000649406.1:c.3129A>T
|
ENSP00000497965.1:p.Glu1043Asp
|
|
|
ENST00000649781.1:c.3129A>T
|
ENSP00000497203.1:p.Glu1043Asp
|
|
|
ENST00000003084.10:c.3312A>T
|
ENSP00000003084.6:p.Glu1104Asp
|
|
|
ENST00000426809.5:c.3222A>T
|
ENSP00000389119.1:p.Glu1074Asp
|
|
|
ENST00000468795.1:c.137A>T
|
|
|
|
NM_000492.3:c.3312A>T , LRG_663t1:c.3312A>T
|
NP_000483.3:p.Glu1104Asp
|
|
|
XM_011515751.1:c.3402A>T
|
XP_011514053.1:p.Glu1134Asp
|
|
|
XM_011515752.1:c.3402A>T
|
XP_011514054.1:p.Glu1134Asp
|
|
|
XM_011515753.1:c.3069A>T
|
XP_011514055.1:p.Glu1023Asp
|
|
|
XM_011515754.1:c.3069A>T
|
XP_011514056.1:p.Glu1023Asp
|
|
|
NM_000492.4:c.3312A>T
MANE Select
|
NP_000483.3:p.Glu1104Asp
|
|
