ENST00000368985.8:c.909C>T
MANE Select
|
ENSP00000357981.3:p.Asn303=
|
|
ENST00000448301.7:c.681C>T
|
ENSP00000408414.2:p.Asn227=
|
|
ENST00000472977.7:c.909C>T
|
ENSP00000475176.2:p.Asn303=
|
|
ENST00000483930.2:c.*103C>T
|
ENSP00000475812.2:n.*103C>T
|
|
ENST00000607427.2:c.909C>T
|
ENSP00000475557.2:p.Asn303=
|
|
ENST00000679512.1:c.806C>T
|
ENSP00000505113.1:p.Thr269Ile
|
|
ENST00000679898.1:c.636C>T
|
ENSP00000505326.1:p.Asn212=
|
|
ENST00000680288.1:c.759C>T
|
ENSP00000506001.1:p.Asn253=
|
|
ENST00000680311.1:c.640C>T
|
ENSP00000505020.1:p.Leu214Phe
|
|
ENST00000680471.1:c.*80C>T
|
ENSP00000506603.1:n.*80C>T
|
|
ENST00000680664.1:c.732C>T
|
ENSP00000506248.1:p.Asn244=
|
|
ENST00000680931.1:c.*259C>T
|
ENSP00000504934.1:n.*259C>T
|
|
ENST00000681357.1:n.299C>T
|
|
|
ENST00000681444.1:c.909C>T
|
ENSP00000505359.1:p.Asn303=
|
|
ENST00000368985.7:c.909C>T
|
ENSP00000357981.3:p.Asn303=
|
|
ENST00000448301.6:c.759C>T
|
ENSP00000408414.1:p.Asn253=
|
|
ENST00000472977.6:c.202C>T
|
|
|
ENST00000483930.1:c.457C>T
|
ENSP00000475812.1:n.457C>T
|
|
NM_001199739.1:c.759C>T
|
NP_001186668.1:p.Asn253=
|
|
NM_004079.4:c.909C>T
|
NP_004070.3:p.Asn303=
|
|
NM_004079.5:c.909C>T
MANE Select
|
NP_004070.3:p.Asn303=
|
|
NM_001199739.2:c.759C>T
|
NP_001186668.1:p.Asn253=
|
|