ENST00000330889.8:c.1070G>A
MANE Select
|
ENSP00000329468.3:p.Arg357Gln
|
|
ENST00000330889.7:c.1070G>A
|
ENSP00000329468.3:p.Arg357Gln
|
|
ENST00000470962.1:n.490G>A
|
|
|
ENST00000480980.1:n.504G>A
|
|
|
ENST00000580525.5:c.1088G>A
|
ENSP00000464121.1:p.Arg363Gln
|
|
ENST00000581285.5:c.986G>A
|
ENSP00000464155.1:p.Arg329Gln
|
|
ENST00000584828.5:c.402+37G>A
|
|
|
ENST00000585130.5:c.*669G>A
|
ENSP00000464120.1:n.*669G>A
|
|
NM_018404.2:c.1070G>A
|
NP_060874.1:p.Arg357Gln
|
|
XM_005258008.2:c.1088G>A
|
XP_005258065.1:p.Arg363Gln
|
|
XM_005258011.2:c.1025G>A
|
XP_005258068.1:p.Arg342Gln
|
|
XM_006721973.2:c.1051+37G>A
|
XP_006722036.1:n.1051+37G>A
|
|
XM_011524993.1:c.1085G>A
|
XP_011523295.1:p.Arg362Gln
|
|
XM_011524994.1:c.1067G>A
|
XP_011523296.1:p.Arg356Gln
|
|
NM_001346712.1:c.1088G>A
|
NP_001333641.1:p.Arg363Gln
|
|
NM_001346714.1:c.1067G>A
|
NP_001333643.1:p.Arg356Gln
|
|
NM_001346716.1:c.1033+37G>A
|
NP_001333645.1:n.1033+37G>A
|
|
NR_144488.1:n.1269G>A
|
|
|
XM_024450831.1:c.1070G>A
|
XP_024306599.1:p.Arg357Gln
|
|
XM_024450832.1:c.1085G>A
|
XP_024306600.1:p.Arg362Gln
|
|
XM_024450833.1:c.1025G>A
|
XP_024306601.1:p.Arg342Gln
|
|
XM_024450834.1:c.1051+37G>A
|
XP_024306602.1:n.1051+37G>A
|
|
XM_024450835.1:c.704G>A
|
XP_024306603.1:p.Arg235Gln
|
|
NM_018404.3:c.1070G>A
MANE Select
|
NP_060874.1:p.Arg357Gln
|
|
NM_001346712.2:c.1088G>A
|
NP_001333641.1:p.Arg363Gln
|
|
NM_001346714.2:c.1067G>A
|
NP_001333643.1:p.Arg356Gln
|
|
NM_001346716.2:c.1033+37G>A
|
NP_001333645.1:n.1033+37G>A
|
|
NR_144488.2:n.1060G>A
|
|
|