ENST00000461574.2:c.5537G=
|
ENSP00000417241.2:p.Cys1846=
|
|
ENST00000470026.6:c.5540G=
|
ENSP00000419274.2:p.Cys1847=
|
|
ENST00000473961.6:c.5414G=
|
ENSP00000420201.2:p.Cys1805=
|
|
ENST00000476777.6:c.5534G=
|
ENSP00000417554.2:p.Cys1845=
|
|
ENST00000477152.6:c.5462G=
|
ENSP00000419988.2:p.Cys1821=
|
|
ENST00000478531.6:c.2228G=
|
ENSP00000420412.2:p.Cys743=
|
|
ENST00000489037.2:c.5462G=
|
ENSP00000420781.2:p.Cys1821=
|
|
ENST00000493919.6:c.2090G=
|
ENSP00000418819.2:p.Cys697=
|
|
ENST00000494123.6:c.5540G=
|
ENSP00000419103.2:p.Cys1847=
|
|
ENST00000497488.2:c.4652G=
|
ENSP00000418986.2:p.Cys1551=
|
|
ENST00000618469.2:c.5540G=
|
ENSP00000478114.2:p.Cys1847=
|
|
ENST00000634433.2:c.5417G=
|
ENSP00000489431.2:p.Cys1806=
|
|
ENST00000644379.2:c.5606G=
|
ENSP00000496570.2:p.Cys1869=
|
|
ENST00000644555.2:c.2090G=
|
ENSP00000494614.2:p.Cys697=
|
|
ENST00000652672.2:c.5399G=
|
ENSP00000498906.2:p.Cys1800=
|
|
ENST00000484087.6:c.2102G=
|
ENSP00000419481.2:p.Cys701=
|
|
ENST00000700081.1:n.1423G=
|
|
|
ENST00000700082.1:n.904G=
|
|
|
ENST00000357654.9:c.5540G=
MANE Select
|
ENSP00000350283.3:p.Cys1847=
|
|
ENST00000471181.7:c.5603G=
|
ENSP00000418960.2:p.Cys1868=
|
|
ENST00000644379.1:c.1927G=
|
|
|
ENST00000352993.7:c.2114G=
|
ENSP00000312236.5:p.Cys705=
|
|
ENST00000357654.7:c.5540G=
|
ENSP00000350283.3:p.Cys1847=
|
|
ENST00000461221.5:c.*5323G=
|
ENSP00000418548.1:n.*5323G=
|
|
ENST00000468300.5:c.*54G=
|
ENSP00000417148.1:n.*54G=
|
|
ENST00000471181.6:c.5603G=
|
ENSP00000418960.2:p.Cys1868=
|
|
ENST00000491747.6:c.2228G=
|
ENSP00000420705.2:p.Cys743=
|
|
ENST00000493795.5:c.5399G=
|
ENSP00000418775.1:p.Cys1800=
|
|
ENST00000586385.5:c.470G=
|
ENSP00000465818.1:p.Cys157=
|
|
ENST00000591534.5:c.1013G=
|
ENSP00000467329.1:p.Cys338=
|
|
ENST00000591849.5:c.239G=
|
ENSP00000465347.1:p.Cys80=
|
|
NM_007294.3:c.5540G= , LRG_292t1:c.5540G=
|
NP_009225.1:p.Cys1847=
|
|
NM_007297.3:c.5399G=
|
NP_009228.2:p.Cys1800=
|
|
NM_007298.3:c.2228G=
|
NP_009229.2:p.Cys743=
|
|
NM_007299.3:c.*54G=
|
NP_009230.2:n.*54G=
|
|
NM_007300.3:c.5603G=
|
NP_009231.2:p.Cys1868=
|
|
NR_027676.1:n.5676G=
|
|
|
NM_007294.4:c.5540G=
MANE Select
|
NP_009225.1:p.Cys1847=
|
|
NM_007297.4:c.5399G=
|
NP_009228.2:p.Cys1800=
|
|
NM_007299.4:c.*54G=
|
NP_009230.2:n.*54G=
|
|
NM_007300.4:c.5603G=
|
NP_009231.2:p.Cys1868=
|
|
NR_027676.2:n.5717G=
|
|
|