ENST00000368985.8:c.927T>G
MANE Select
|
ENSP00000357981.3:p.Tyr309Ter
|
|
ENST00000448301.7:c.699T>G
|
ENSP00000408414.2:p.Tyr233Ter
|
|
ENST00000472977.7:c.927T>G
|
ENSP00000475176.2:p.Tyr309Ter
|
|
ENST00000483930.2:c.*121T>G
|
ENSP00000475812.2:n.*121T>G
|
|
ENST00000607427.2:c.927T>G
|
ENSP00000475557.2:p.Tyr309Ter
|
|
ENST00000679512.1:c.824T>G
|
ENSP00000505113.1:p.Ile275Arg
|
|
ENST00000679898.1:c.654T>G
|
ENSP00000505326.1:p.Tyr218Ter
|
|
ENST00000680288.1:c.777T>G
|
ENSP00000506001.1:p.Tyr259Ter
|
|
ENST00000680311.1:c.*10T>G
|
ENSP00000505020.1:n.*10T>G
|
|
ENST00000680471.1:c.*98T>G
|
ENSP00000506603.1:n.*98T>G
|
|
ENST00000680664.1:c.750T>G
|
ENSP00000506248.1:p.Tyr250Ter
|
|
ENST00000680931.1:c.*277T>G
|
ENSP00000504934.1:n.*277T>G
|
|
ENST00000681357.1:n.317T>G
|
|
|
ENST00000681444.1:c.927T>G
|
ENSP00000505359.1:p.Tyr309Ter
|
|
ENST00000368985.7:c.927T>G
|
ENSP00000357981.3:p.Tyr309Ter
|
|
ENST00000448301.6:c.777T>G
|
ENSP00000408414.1:p.Tyr259Ter
|
|
ENST00000472977.6:c.220T>G
|
|
|
ENST00000483930.1:c.475T>G
|
ENSP00000475812.1:n.475T>G
|
|
NM_001199739.1:c.777T>G
|
NP_001186668.1:p.Tyr259Ter
|
|
NM_004079.4:c.927T>G
|
NP_004070.3:p.Tyr309Ter
|
|
NM_004079.5:c.927T>G
MANE Select
|
NP_004070.3:p.Tyr309Ter
|
|
NM_001199739.2:c.777T>G
|
NP_001186668.1:p.Tyr259Ter
|
|