ENST00000368985.8:c.925T>A
MANE Select
|
ENSP00000357981.3:p.Tyr309Asn
|
|
ENST00000448301.7:c.697T>A
|
ENSP00000408414.2:p.Tyr233Asn
|
|
ENST00000472977.7:c.925T>A
|
ENSP00000475176.2:p.Tyr309Asn
|
|
ENST00000483930.2:c.*119T>A
|
ENSP00000475812.2:n.*119T>A
|
|
ENST00000607427.2:c.925T>A
|
ENSP00000475557.2:p.Tyr309Asn
|
|
ENST00000679512.1:c.822T>A
|
ENSP00000505113.1:p.Asp274Glu
|
|
ENST00000679898.1:c.652T>A
|
ENSP00000505326.1:p.Tyr218Asn
|
|
ENST00000680288.1:c.775T>A
|
ENSP00000506001.1:p.Tyr259Asn
|
|
ENST00000680311.1:c.*8T>A
|
ENSP00000505020.1:n.*8T>A
|
|
ENST00000680471.1:c.*96T>A
|
ENSP00000506603.1:n.*96T>A
|
|
ENST00000680664.1:c.748T>A
|
ENSP00000506248.1:p.Tyr250Asn
|
|
ENST00000680931.1:c.*275T>A
|
ENSP00000504934.1:n.*275T>A
|
|
ENST00000681357.1:n.315T>A
|
|
|
ENST00000681444.1:c.925T>A
|
ENSP00000505359.1:p.Tyr309Asn
|
|
ENST00000368985.7:c.925T>A
|
ENSP00000357981.3:p.Tyr309Asn
|
|
ENST00000448301.6:c.775T>A
|
ENSP00000408414.1:p.Tyr259Asn
|
|
ENST00000472977.6:c.218T>A
|
|
|
ENST00000483930.1:c.473T>A
|
ENSP00000475812.1:n.473T>A
|
|
NM_001199739.1:c.775T>A
|
NP_001186668.1:p.Tyr259Asn
|
|
NM_004079.4:c.925T>A
|
NP_004070.3:p.Tyr309Asn
|
|
NM_004079.5:c.925T>A
MANE Select
|
NP_004070.3:p.Tyr309Asn
|
|
NM_001199739.2:c.775T>A
|
NP_001186668.1:p.Tyr259Asn
|
|