ENST00000368985.8:c.996G>C
MANE Select
|
ENSP00000357981.3:p.Ter332Tyr
|
|
ENST00000448301.7:c.768G>C
|
ENSP00000408414.2:p.Ter256Tyr
|
|
ENST00000472977.7:c.996G>C
|
ENSP00000475176.2:p.Ter332Tyr
|
|
ENST00000483930.2:c.*190G>C
|
ENSP00000475812.2:n.*190G>C
|
|
ENST00000607427.2:c.996G>C
|
ENSP00000475557.2:p.Ter332Tyr
|
|
ENST00000679512.1:c.893G>C
|
ENSP00000505113.1:p.Arg298Thr
|
|
ENST00000679898.1:c.723G>C
|
ENSP00000505326.1:p.Ter241Tyr
|
|
ENST00000680288.1:c.846G>C
|
ENSP00000506001.1:p.Ter282Tyr
|
|
ENST00000680311.1:c.*79G>C
|
ENSP00000505020.1:n.*79G>C
|
|
ENST00000680471.1:c.*167G>C
|
ENSP00000506603.1:n.*167G>C
|
|
ENST00000680664.1:c.819G>C
|
ENSP00000506248.1:p.Ter273Tyr
|
|
ENST00000680931.1:c.*346G>C
|
ENSP00000504934.1:n.*346G>C
|
|
ENST00000681357.1:n.386G>C
|
|
|
ENST00000681444.1:c.996G>C
|
ENSP00000505359.1:p.Ter332Tyr
|
|
ENST00000368985.7:c.996G>C
|
ENSP00000357981.3:p.Ter332Tyr
|
|
ENST00000448301.6:c.846G>C
|
ENSP00000408414.1:p.Ter282Tyr
|
|
ENST00000472977.6:c.289G>C
|
|
|
ENST00000483930.1:c.544G>C
|
ENSP00000475812.1:n.544G>C
|
|
ENST00000607427.1:c.17G>C
|
|
|
NM_001199739.1:c.846G>C
|
NP_001186668.1:p.Ter282Tyr
|
|
NM_004079.4:c.996G>C
|
NP_004070.3:p.Ter332Tyr
|
|
NM_004079.5:c.996G>C
MANE Select
|
NP_004070.3:p.Ter332Tyr
|
|
NM_001199739.2:c.846G>C
|
NP_001186668.1:p.Ter282Tyr
|
|