ENST00000368985.8:c.917A>T
MANE Select
|
ENSP00000357981.3:p.Glu306Val
|
|
ENST00000448301.7:c.689A>T
|
ENSP00000408414.2:p.Glu230Val
|
|
ENST00000472977.7:c.917A>T
|
ENSP00000475176.2:p.Glu306Val
|
|
ENST00000483930.2:c.*111A>T
|
ENSP00000475812.2:n.*111A>T
|
|
ENST00000607427.2:c.917A>T
|
ENSP00000475557.2:p.Glu306Val
|
|
ENST00000679512.1:c.814A>T
|
ENSP00000505113.1:p.Lys272Ter
|
|
ENST00000679898.1:c.644A>T
|
ENSP00000505326.1:p.Glu215Val
|
|
ENST00000680288.1:c.767A>T
|
ENSP00000506001.1:p.Glu256Val
|
|
ENST00000680311.1:c.648A>T
|
ENSP00000505020.1:p.Ter216Cys
|
|
ENST00000680471.1:c.*88A>T
|
ENSP00000506603.1:n.*88A>T
|
|
ENST00000680664.1:c.740A>T
|
ENSP00000506248.1:p.Glu247Val
|
|
ENST00000680931.1:c.*267A>T
|
ENSP00000504934.1:n.*267A>T
|
|
ENST00000681357.1:n.307A>T
|
|
|
ENST00000681444.1:c.917A>T
|
ENSP00000505359.1:p.Glu306Val
|
|
ENST00000368985.7:c.917A>T
|
ENSP00000357981.3:p.Glu306Val
|
|
ENST00000448301.6:c.767A>T
|
ENSP00000408414.1:p.Glu256Val
|
|
ENST00000472977.6:c.210A>T
|
|
|
ENST00000483930.1:c.465A>T
|
ENSP00000475812.1:n.465A>T
|
|
NM_001199739.1:c.767A>T
|
NP_001186668.1:p.Glu256Val
|
|
NM_004079.4:c.917A>T
|
NP_004070.3:p.Glu306Val
|
|
NM_004079.5:c.917A>T
MANE Select
|
NP_004070.3:p.Glu306Val
|
|
NM_001199739.2:c.767A>T
|
NP_001186668.1:p.Glu256Val
|
|