|
ENST00000647720.2:c.2816A>G
|
ENSP00000497673.2:p.His939Arg
|
|
|
ENST00000647978.2:c.*2530A>G
|
ENSP00000497658.1:n.*2530A>G
|
|
|
ENST00000649781.2:c.2633A>G
|
ENSP00000497203.1:p.His878Arg
|
|
|
ENST00000685018.2:c.2816A>G
|
ENSP00000510194.2:p.His939Arg
|
|
|
ENST00000687278.2:c.2816A>G
|
ENSP00000509593.2:p.His939Arg
|
|
|
ENST00000699585.1:c.2816A>G
|
ENSP00000514456.1:p.His939Arg
|
|
|
ENST00000699598.1:c.2816A>G
|
ENSP00000514467.1:p.His939Arg
|
|
|
ENST00000699599.1:c.2816A>G
|
ENSP00000514468.1:p.His939Arg
|
|
|
ENST00000699600.1:c.2816A>G
|
ENSP00000514469.1:p.His939Arg
|
|
|
ENST00000699601.1:c.*1116A>G
|
ENSP00000514470.1:n.*1116A>G
|
|
|
ENST00000699602.1:c.2816A>G
|
ENSP00000514471.1:p.His939Arg
|
|
|
ENST00000699604.1:c.*2640A>G
|
ENSP00000514472.1:n.*2640A>G
|
|
|
ENST00000699605.1:c.2390A>G
|
ENSP00000514473.1:p.His797Arg
|
|
|
ENST00000687278.1:c.407A>G
|
ENSP00000509593.1:p.His136Arg
|
|
|
ENST00000003084.11:c.2816A>G
MANE Select
|
ENSP00000003084.6:p.His939Arg
|
|
|
ENST00000647720.1:c.466A>G
|
|
|
|
ENST00000648260.1:c.1598A>G
|
ENSP00000497957.1:p.His533Arg
|
|
|
ENST00000649406.1:c.2633A>G
|
ENSP00000497965.1:p.His878Arg
|
|
|
ENST00000649781.1:c.2633A>G
|
ENSP00000497203.1:p.His878Arg
|
|
|
ENST00000003084.10:c.2816A>G
|
ENSP00000003084.6:p.His939Arg
|
|
|
ENST00000426809.5:c.2726A>G
|
ENSP00000389119.1:p.His909Arg
|
|
|
NM_000492.3:c.2816A>G , LRG_663t1:c.2816A>G
|
NP_000483.3:p.His939Arg
|
|
|
XM_011515751.1:c.2906A>G
|
XP_011514053.1:p.His969Arg
|
|
|
XM_011515752.1:c.2906A>G
|
XP_011514054.1:p.His969Arg
|
|
|
XM_011515753.1:c.2573A>G
|
XP_011514055.1:p.His858Arg
|
|
|
XM_011515754.1:c.2573A>G
|
XP_011514056.1:p.His858Arg
|
|
|
NM_000492.4:c.2816A>G
MANE Select
|
NP_000483.3:p.His939Arg
|
|
