ENST00000461574.2:c.5454T>C
|
ENSP00000417241.2:p.Asn1818=
|
|
ENST00000470026.6:c.5457T>C
|
ENSP00000419274.2:p.Asn1819=
|
|
ENST00000473961.6:c.5331T>C
|
ENSP00000420201.2:p.Asn1777=
|
|
ENST00000476777.6:c.5451T>C
|
ENSP00000417554.2:p.Asn1817=
|
|
ENST00000477152.6:c.5379T>C
|
ENSP00000419988.2:p.Asn1793=
|
|
ENST00000478531.6:c.2145T>C
|
ENSP00000420412.2:p.Asn715=
|
|
ENST00000489037.2:c.5379T>C
|
ENSP00000420781.2:p.Asn1793=
|
|
ENST00000493919.6:c.2007T>C
|
ENSP00000418819.2:p.Asn669=
|
|
ENST00000494123.6:c.5457T>C
|
ENSP00000419103.2:p.Asn1819=
|
|
ENST00000497488.2:c.4569T>C
|
ENSP00000418986.2:p.Asn1523=
|
|
ENST00000618469.2:c.5457T>C
|
ENSP00000478114.2:p.Asn1819=
|
|
ENST00000634433.2:c.5334T>C
|
ENSP00000489431.2:p.Asn1778=
|
|
ENST00000644379.2:c.5523T>C
|
ENSP00000496570.2:p.Asn1841=
|
|
ENST00000644555.2:c.2007T>C
|
ENSP00000494614.2:p.Asn669=
|
|
ENST00000652672.2:c.5316T>C
|
ENSP00000498906.2:p.Asn1772=
|
|
ENST00000484087.6:c.2019T>C
|
ENSP00000419481.2:p.Asn673=
|
|
ENST00000700081.1:n.1340T>C
|
|
|
ENST00000700082.1:n.821T>C
|
|
|
ENST00000357654.9:c.5457T>C
MANE Select
|
ENSP00000350283.3:p.Asn1819=
|
|
ENST00000471181.7:c.5520T>C
|
ENSP00000418960.2:p.Asn1840=
|
|
ENST00000644379.1:c.1844T>C
|
|
|
ENST00000352993.7:c.2031T>C
|
ENSP00000312236.5:p.Asn677=
|
|
ENST00000357654.7:c.5457T>C
|
ENSP00000350283.3:p.Asn1819=
|
|
ENST00000461221.5:c.*5240T>C
|
ENSP00000418548.1:n.*5240T>C
|
|
ENST00000468300.5:c.2071T>C
|
ENSP00000417148.1:p.Trp691Arg
|
|
ENST00000471181.6:c.5520T>C
|
ENSP00000418960.2:p.Asn1840=
|
|
ENST00000491747.6:c.2145T>C
|
ENSP00000420705.2:p.Asn715=
|
|
ENST00000493795.5:c.5316T>C
|
ENSP00000418775.1:p.Asn1772=
|
|
ENST00000586385.5:c.387T>C
|
ENSP00000465818.1:p.Asn129=
|
|
ENST00000591534.5:c.930T>C
|
ENSP00000467329.1:p.Asn310=
|
|
ENST00000591849.5:c.156T>C
|
ENSP00000465347.1:p.Asn52=
|
|
NM_007294.3:c.5457T>C , LRG_292t1:c.5457T>C
|
NP_009225.1:p.Asn1819=
|
|
NM_007297.3:c.5316T>C
|
NP_009228.2:p.Asn1772=
|
|
NM_007298.3:c.2145T>C
|
NP_009229.2:p.Asn715=
|
|
NM_007299.3:c.2071T>C
|
NP_009230.2:p.Trp691Arg
|
|
NM_007300.3:c.5520T>C
|
NP_009231.2:p.Asn1840=
|
|
NR_027676.1:n.5593T>C
|
|
|
NM_007294.4:c.5457T>C
MANE Select
|
NP_009225.1:p.Asn1819=
|
|
NM_007297.4:c.5316T>C
|
NP_009228.2:p.Asn1772=
|
|
NM_007299.4:c.2071T>C
|
NP_009230.2:p.Trp691Arg
|
|
NM_007300.4:c.5520T>C
|
NP_009231.2:p.Asn1840=
|
|
NR_027676.2:n.5634T>C
|
|
|