ENST00000330889.8:c.1024A=
MANE Select
|
ENSP00000329468.3:p.Thr342=
|
|
ENST00000330889.7:c.1024A=
|
ENSP00000329468.3:p.Thr342=
|
|
ENST00000470962.1:n.444A=
|
|
|
ENST00000480980.1:n.458A=
|
|
|
ENST00000580525.5:c.1042A=
|
ENSP00000464121.1:p.Thr348=
|
|
ENST00000581285.5:c.940A=
|
ENSP00000464155.1:p.Thr314=
|
|
ENST00000584828.5:c.393A=
|
|
|
ENST00000585130.5:c.*623A=
|
ENSP00000464120.1:n.*623A=
|
|
NM_018404.2:c.1024A=
|
NP_060874.1:p.Thr342=
|
|
XM_005258008.2:c.1042A=
|
XP_005258065.1:p.Thr348=
|
|
XM_005258011.2:c.979A=
|
XP_005258068.1:p.Thr327=
|
|
XM_006721973.2:c.1042A=
|
XP_006722036.1:p.Thr348=
|
|
XM_011524993.1:c.1039A=
|
XP_011523295.1:p.Thr347=
|
|
XM_011524994.1:c.1021A=
|
XP_011523296.1:p.Thr341=
|
|
NM_001346712.1:c.1042A=
|
NP_001333641.1:p.Thr348=
|
|
NM_001346714.1:c.1021A=
|
NP_001333643.1:p.Thr341=
|
|
NM_001346716.1:c.1024A=
|
NP_001333645.1:p.Thr342=
|
|
NR_144488.1:n.1223A=
|
|
|
XM_024450831.1:c.1024A=
|
XP_024306599.1:p.Thr342=
|
|
XM_024450832.1:c.1039A=
|
XP_024306600.1:p.Thr347=
|
|
XM_024450833.1:c.979A=
|
XP_024306601.1:p.Thr327=
|
|
XM_024450834.1:c.1042A=
|
XP_024306602.1:p.Thr348=
|
|
XM_024450835.1:c.658A=
|
XP_024306603.1:p.Thr220=
|
|
NM_018404.3:c.1024A=
MANE Select
|
NP_060874.1:p.Thr342=
|
|
NM_001346712.2:c.1042A=
|
NP_001333641.1:p.Thr348=
|
|
NM_001346714.2:c.1021A=
|
NP_001333643.1:p.Thr341=
|
|
NM_001346716.2:c.1024A=
|
NP_001333645.1:p.Thr342=
|
|
NR_144488.2:n.1014A=
|
|
|