ENST00000391944.8:c.2099A>G
|
ENSP00000375808.4:p.His700Arg
|
|
ENST00000682414.1:c.2099A>G
|
ENSP00000507019.1:p.His700Arg
|
|
ENST00000682508.1:n.2128A>G
|
|
|
ENST00000684218.1:c.*1357A>G
|
ENSP00000507804.1:n.*1357A>G
|
|
ENST00000684264.1:n.1655A>G
|
|
|
ENST00000684407.1:c.1976A>G
|
ENSP00000507775.1:p.His659Arg
|
|
ENST00000684458.1:c.*585A>G
|
ENSP00000508260.1:n.*585A>G
|
|
ENST00000684468.1:n.1811A>G
|
|
|
ENST00000391945.10:c.2099A>G
MANE Select
|
ENSP00000375809.4:p.His700Arg
|
|
ENST00000646507.1:n.2196A>G
|
|
|
ENST00000391941.6:c.2027A>G
|
ENSP00000375805.2:p.His676Arg
|
|
ENST00000391942.6:n.1270A>G
|
|
|
ENST00000391944.7:c.1865A>G
|
ENSP00000375808.3:p.His622Arg
|
|
ENST00000391945.8:c.2099A>G
|
ENSP00000375809.3:p.His700Arg
|
|
ENST00000588652.5:n.2187A>G
|
|
|
NM_000400.3:c.2099A>G , LRG_461t1:c.2099A>G
|
NP_000391.1:p.His700Arg
|
|
XM_011526611.1:c.2021A>G
|
XP_011524913.1:p.His674Arg
|
|
XM_011526611.2:c.2021A>G
|
XP_011524913.1:p.His674Arg
|
|
XM_017026467.1:c.1976A>G
|
XP_016881956.1:p.His659Arg
|
|
XR_001753633.2:n.2146A>G
|
|
|
XR_001753634.2:n.2082A>G
|
|
|
NM_000400.4:c.2099A>G
MANE Select
|
NP_000391.1:p.His700Arg
|
|