ENST00000263967.4:c.3068G>A
MANE Select
|
ENSP00000263967.3:p.Arg1023Gln
|
|
ENST00000462255.2:n.2091G>A
|
|
|
ENST00000643187.1:c.*148G>A
|
ENSP00000493507.1:n.*148G>A
|
|
ENST00000674534.1:n.3976G>A
|
|
|
ENST00000674622.1:c.1489G>A
|
ENSP00000502417.1:n.1489G>A
|
|
ENST00000675467.1:n.5875G>A
|
|
|
ENST00000675786.1:c.*1635G>A
|
ENSP00000502323.1:n.*1635G>A
|
|
ENST00000675796.1:n.2963G>A
|
|
|
ENST00000263967.3:c.3068G>A
|
ENSP00000263967.3:p.Arg1023Gln
|
|
NM_006218.2:c.3068G>A , LRG_310t1:c.3068G>A
|
NP_006209.2:p.Arg1023Gln
|
|
XM_006713658.2:c.3068G>A
|
XP_006713721.1:p.Arg1023Gln
|
|
XM_011512894.1:c.3068G>A
|
XP_011511196.1:p.Arg1023Gln
|
|
NM_006218.3:c.3068G>A
|
NP_006209.2:p.Arg1023Gln
|
|
XM_006713658.4:c.3068G>A
|
XP_006713721.1:p.Arg1023Gln
|
|
XM_011512894.2:c.3068G>A
|
XP_011511196.1:p.Arg1023Gln
|
|
NM_006218.4:c.3068G>A
MANE Select
|
NP_006209.2:p.Arg1023Gln
|
|