ENST00000700075.1:c.44A>G
|
ENSP00000514784.1:p.Gln15Arg
|
|
ENST00000342771.10:c.1976A>G
MANE Select
|
ENSP00000344087.4:p.Gln659Arg
|
|
ENST00000439256.2:c.74A>G
|
ENSP00000407058.2:p.Gln25Arg
|
|
ENST00000443672.2:c.311A>G
|
ENSP00000393548.2:p.Gln104Arg
|
|
ENST00000449547.6:c.69A>G
|
|
|
ENST00000464768.2:n.644A>G
|
|
|
ENST00000644359.1:c.557A>G
|
ENSP00000494561.1:p.Gln186Arg
|
|
ENST00000644506.1:c.602A>G
|
ENSP00000496672.1:p.Gln201Arg
|
|
ENST00000644939.1:c.1973A>G
|
ENSP00000496726.1:p.Gln658Arg
|
|
ENST00000646136.1:n.287A>G
|
|
|
ENST00000647140.1:c.841A>G
|
|
|
ENST00000342771.8:c.1976A>G
|
ENSP00000344087.4:p.Gln659Arg
|
|
ENST00000406775.6:c.1904A>G
|
ENSP00000385263.2:p.Gln635Arg
|
|
ENST00000439256.1:c.74A>G
|
|
|
ENST00000464768.1:n.642A>G
|
|
|
ENST00000465899.1:n.473A>G
|
|
|
ENST00000498384.5:n.344A>G
|
|
|
ENST00000611706.4:c.1232A>G
|
ENSP00000478134.1:p.Gln411Arg
|
|
ENST00000615871.4:c.1160A>G
|
ENSP00000479325.1:p.Gln387Arg
|
|
NM_001127231.2:c.1904A>G
|
NP_001120703.1:p.Gln635Arg
|
|
NM_015570.3:c.1976A>G
|
NP_056385.1:p.Gln659Arg
|
|
XM_005250257.1:c.623A>G
|
XP_005250314.1:p.Gln208Arg
|
|
XM_011516010.1:c.1997A>G
|
XP_011514312.1:p.Gln666Arg
|
|
XM_011516011.1:c.1994A>G
|
XP_011514313.1:p.Gln665Arg
|
|
XM_011516012.1:c.1931A>G
|
XP_011514314.1:p.Gln644Arg
|
|
XM_011516013.1:c.1925A>G
|
XP_011514315.1:p.Gln642Arg
|
|
XM_011516014.1:c.1895A>G
|
XP_011514316.1:p.Gln632Arg
|
|
XM_011516015.1:c.1733A>G
|
XP_011514317.1:p.Gln578Arg
|
|
XM_011516016.1:c.1706A>G
|
XP_011514318.1:p.Gln569Arg
|
|
XM_011516017.1:c.1523A>G
|
XP_011514319.1:p.Gln508Arg
|
|
XM_011516018.1:c.1496A>G
|
XP_011514320.1:p.Gln499Arg
|
|
XM_005250257.2:c.623A>G
|
XP_005250314.1:p.Gln208Arg
|
|
XM_011516010.2:c.1997A>G
|
XP_011514312.1:p.Gln666Arg
|
|
XM_011516011.2:c.1994A>G
|
XP_011514313.1:p.Gln665Arg
|
|
XM_011516012.2:c.1931A>G
|
XP_011514314.1:p.Gln644Arg
|
|
XM_011516013.2:c.1925A>G
|
XP_011514315.1:p.Gln642Arg
|
|
XM_011516014.2:c.1895A>G
|
XP_011514316.1:p.Gln632Arg
|
|
XM_011516017.2:c.1523A>G
|
XP_011514319.1:p.Gln508Arg
|
|
XM_011516018.2:c.1496A>G
|
XP_011514320.1:p.Gln499Arg
|
|
XM_017011951.2:c.1997A>G
|
XP_016867440.1:p.Gln666Arg
|
|
NM_001127231.3:c.1904A>G
|
NP_001120703.1:p.Gln635Arg
|
|
NM_015570.4:c.1976A>G
MANE Select
|
NP_056385.1:p.Gln659Arg
|
|