ENST00000368985.8:c.920A>T
MANE Select
|
ENSP00000357981.3:p.Glu307Val
|
|
ENST00000448301.7:c.692A>T
|
ENSP00000408414.2:p.Glu231Val
|
|
ENST00000472977.7:c.920A>T
|
ENSP00000475176.2:p.Glu307Val
|
|
ENST00000483930.2:c.*114A>T
|
ENSP00000475812.2:n.*114A>T
|
|
ENST00000607427.2:c.920A>T
|
ENSP00000475557.2:p.Glu307Val
|
|
ENST00000679512.1:c.817A>T
|
ENSP00000505113.1:p.Lys273Ter
|
|
ENST00000679898.1:c.647A>T
|
ENSP00000505326.1:p.Glu216Val
|
|
ENST00000680288.1:c.770A>T
|
ENSP00000506001.1:p.Glu257Val
|
|
ENST00000680311.1:c.*3A>T
|
ENSP00000505020.1:n.*3A>T
|
|
ENST00000680471.1:c.*91A>T
|
ENSP00000506603.1:n.*91A>T
|
|
ENST00000680664.1:c.743A>T
|
ENSP00000506248.1:p.Glu248Val
|
|
ENST00000680931.1:c.*270A>T
|
ENSP00000504934.1:n.*270A>T
|
|
ENST00000681357.1:n.310A>T
|
|
|
ENST00000681444.1:c.920A>T
|
ENSP00000505359.1:p.Glu307Val
|
|
ENST00000368985.7:c.920A>T
|
ENSP00000357981.3:p.Glu307Val
|
|
ENST00000448301.6:c.770A>T
|
ENSP00000408414.1:p.Glu257Val
|
|
ENST00000472977.6:c.213A>T
|
|
|
ENST00000483930.1:c.468A>T
|
ENSP00000475812.1:n.468A>T
|
|
NM_001199739.1:c.770A>T
|
NP_001186668.1:p.Glu257Val
|
|
NM_004079.4:c.920A>T
|
NP_004070.3:p.Glu307Val
|
|
NM_004079.5:c.920A>T
MANE Select
|
NP_004070.3:p.Glu307Val
|
|
NM_001199739.2:c.770A>T
|
NP_001186668.1:p.Glu257Val
|
|