ENST00000368985.8:c.953A>G
MANE Select
|
ENSP00000357981.3:p.Asn318Ser
|
|
ENST00000448301.7:c.725A>G
|
ENSP00000408414.2:p.Asn242Ser
|
|
ENST00000472977.7:c.953A>G
|
ENSP00000475176.2:p.Asn318Ser
|
|
ENST00000483930.2:c.*147A>G
|
ENSP00000475812.2:n.*147A>G
|
|
ENST00000607427.2:c.953A>G
|
ENSP00000475557.2:p.Asn318Ser
|
|
ENST00000679512.1:c.850A>G
|
ENSP00000505113.1:p.Ile284Val
|
|
ENST00000679898.1:c.680A>G
|
ENSP00000505326.1:p.Asn227Ser
|
|
ENST00000680288.1:c.803A>G
|
ENSP00000506001.1:p.Asn268Ser
|
|
ENST00000680311.1:c.*36A>G
|
ENSP00000505020.1:n.*36A>G
|
|
ENST00000680471.1:c.*124A>G
|
ENSP00000506603.1:n.*124A>G
|
|
ENST00000680664.1:c.776A>G
|
ENSP00000506248.1:p.Asn259Ser
|
|
ENST00000680931.1:c.*303A>G
|
ENSP00000504934.1:n.*303A>G
|
|
ENST00000681357.1:n.343A>G
|
|
|
ENST00000681444.1:c.953A>G
|
ENSP00000505359.1:p.Asn318Ser
|
|
ENST00000368985.7:c.953A>G
|
ENSP00000357981.3:p.Asn318Ser
|
|
ENST00000448301.6:c.803A>G
|
ENSP00000408414.1:p.Asn268Ser
|
|
ENST00000472977.6:c.246A>G
|
|
|
ENST00000483930.1:c.501A>G
|
ENSP00000475812.1:n.501A>G
|
|
NM_001199739.1:c.803A>G
|
NP_001186668.1:p.Asn268Ser
|
|
NM_004079.4:c.953A>G
|
NP_004070.3:p.Asn318Ser
|
|
NM_004079.5:c.953A>G
MANE Select
|
NP_004070.3:p.Asn318Ser
|
|
NM_001199739.2:c.803A>G
|
NP_001186668.1:p.Asn268Ser
|
|