ENST00000368985.8:c.907A>G
MANE Select
|
ENSP00000357981.3:p.Asn303Asp
|
|
ENST00000448301.7:c.679A>G
|
ENSP00000408414.2:p.Asn227Asp
|
|
ENST00000472977.7:c.907A>G
|
ENSP00000475176.2:p.Asn303Asp
|
|
ENST00000483930.2:c.*101A>G
|
ENSP00000475812.2:n.*101A>G
|
|
ENST00000607427.2:c.907A>G
|
ENSP00000475557.2:p.Asn303Asp
|
|
ENST00000679512.1:c.804A>G
|
ENSP00000505113.1:p.Thr268=
|
|
ENST00000679898.1:c.634A>G
|
ENSP00000505326.1:p.Asn212Asp
|
|
ENST00000680288.1:c.757A>G
|
ENSP00000506001.1:p.Asn253Asp
|
|
ENST00000680311.1:c.638A>G
|
ENSP00000505020.1:p.Gln213Arg
|
|
ENST00000680471.1:c.*78A>G
|
ENSP00000506603.1:n.*78A>G
|
|
ENST00000680664.1:c.730A>G
|
ENSP00000506248.1:p.Asn244Asp
|
|
ENST00000680931.1:c.*257A>G
|
ENSP00000504934.1:n.*257A>G
|
|
ENST00000681357.1:n.297A>G
|
|
|
ENST00000681444.1:c.907A>G
|
ENSP00000505359.1:p.Asn303Asp
|
|
ENST00000368985.7:c.907A>G
|
ENSP00000357981.3:p.Asn303Asp
|
|
ENST00000448301.6:c.757A>G
|
ENSP00000408414.1:p.Asn253Asp
|
|
ENST00000472977.6:c.200A>G
|
|
|
ENST00000483930.1:c.455A>G
|
ENSP00000475812.1:n.455A>G
|
|
NM_001199739.1:c.757A>G
|
NP_001186668.1:p.Asn253Asp
|
|
NM_004079.4:c.907A>G
|
NP_004070.3:p.Asn303Asp
|
|
NM_004079.5:c.907A>G
MANE Select
|
NP_004070.3:p.Asn303Asp
|
|
NM_001199739.2:c.757A>G
|
NP_001186668.1:p.Asn253Asp
|
|