ENST00000304895.9:c.1953T>A
MANE Select
|
ENSP00000302728.4:p.Thr651=
|
|
ENST00000304895.8:c.1953T>A
|
ENSP00000302728.4:p.Thr651=
|
|
ENST00000421103.5:c.1515T>A
|
ENSP00000391390.1:p.Thr505=
|
|
ENST00000430730.5:c.*1220T>A
|
ENSP00000411859.1:n.*1220T>A
|
|
ENST00000447929.5:c.*1333T>A
|
ENSP00000411262.1:n.*1333T>A
|
|
ENST00000466883.5:n.2343T>A
|
|
|
NM_000181.3:c.1953T>A
|
NP_000172.2:p.Thr651=
|
|
NM_001284290.1:c.1515T>A
|
NP_001271219.1:p.Thr505=
|
|
NM_001293104.1:c.1383T>A
|
NP_001280033.1:p.Thr461=
|
|
NM_001293105.1:c.1296T>A
|
NP_001280034.1:p.Thr432=
|
|
NR_120531.1:n.1999T>A
|
|
|
XM_005250297.3:c.1800T>A
|
XP_005250354.1:p.Thr600=
|
|
XM_011516113.1:c.1452T>A
|
XP_011514415.1:p.Thr484=
|
|
XM_011516114.1:c.1281T>A
|
XP_011514416.1:p.Thr427=
|
|
XM_005250297.4:c.1800T>A
|
XP_005250354.1:p.Thr600=
|
|
XM_011516114.2:c.1281T>A
|
XP_011514416.1:p.Thr427=
|
|
XM_017012091.1:c.1299T>A
|
XP_016867580.1:p.Thr433=
|
|
XM_017012092.1:c.1230T>A
|
XP_016867581.1:p.Thr410=
|
|
XM_017012093.2:c.1128T>A
|
XP_016867582.1:p.Thr376=
|
|
XR_001744658.2:n.1760T>A
|
|
|
XR_001744659.2:n.1873T>A
|
|
|
XR_001744660.2:n.1805T>A
|
|
|
XR_001744661.2:n.1720T>A
|
|
|
XR_927461.3:n.1958T>A
|
|
|
NM_000181.4:c.1953T>A
MANE Select
|
NP_000172.2:p.Thr651=
|
|
NM_001284290.2:c.1515T>A
|
NP_001271219.1:p.Thr505=
|
|
NM_001293104.2:c.1383T>A
|
NP_001280033.1:p.Thr461=
|
|
NM_001293105.2:c.1296T>A
|
NP_001280034.1:p.Thr432=
|
|
NR_120531.2:n.1898T>A
|
|
|