ENST00000461574.2:c.5417T>A
|
ENSP00000417241.2:p.Ile1806Asn
|
|
ENST00000470026.6:c.5420T>A
|
ENSP00000419274.2:p.Ile1807Asn
|
|
ENST00000473961.6:c.5294T>A
|
ENSP00000420201.2:p.Ile1765Asn
|
|
ENST00000476777.6:c.5414T>A
|
ENSP00000417554.2:p.Ile1805Asn
|
|
ENST00000477152.6:c.5342T>A
|
ENSP00000419988.2:p.Ile1781Asn
|
|
ENST00000478531.6:c.2108T>A
|
ENSP00000420412.2:p.Ile703Asn
|
|
ENST00000489037.2:c.5342T>A
|
ENSP00000420781.2:p.Ile1781Asn
|
|
ENST00000493919.6:c.1970T>A
|
ENSP00000418819.2:p.Ile657Asn
|
|
ENST00000494123.6:c.5420T>A
|
ENSP00000419103.2:p.Ile1807Asn
|
|
ENST00000497488.2:c.4532T>A
|
ENSP00000418986.2:p.Ile1511Asn
|
|
ENST00000618469.2:c.5420T>A
|
ENSP00000478114.2:p.Ile1807Asn
|
|
ENST00000634433.2:c.5297T>A
|
ENSP00000489431.2:p.Ile1766Asn
|
|
ENST00000644379.2:c.5486T>A
|
ENSP00000496570.2:p.Ile1829Asn
|
|
ENST00000644555.2:c.1970T>A
|
ENSP00000494614.2:p.Ile657Asn
|
|
ENST00000652672.2:c.5279T>A
|
ENSP00000498906.2:p.Ile1760Asn
|
|
ENST00000484087.6:c.1982T>A
|
ENSP00000419481.2:p.Ile661Asn
|
|
ENST00000700081.1:n.1303T>A
|
|
|
ENST00000700082.1:n.784T>A
|
|
|
ENST00000357654.9:c.5420T>A
MANE Select
|
ENSP00000350283.3:p.Ile1807Asn
|
|
ENST00000471181.7:c.5483T>A
|
ENSP00000418960.2:p.Ile1828Asn
|
|
ENST00000644379.1:c.1807T>A
|
|
|
ENST00000352993.7:c.1994T>A
|
ENSP00000312236.5:p.Ile665Asn
|
|
ENST00000357654.7:c.5420T>A
|
ENSP00000350283.3:p.Ile1807Asn
|
|
ENST00000461221.5:c.*5203T>A
|
ENSP00000418548.1:n.*5203T>A
|
|
ENST00000468300.5:c.2034T>A
|
ENSP00000417148.1:p.Asn678Lys
|
|
ENST00000471181.6:c.5483T>A
|
ENSP00000418960.2:p.Ile1828Asn
|
|
ENST00000491747.6:c.2108T>A
|
ENSP00000420705.2:p.Ile703Asn
|
|
ENST00000493795.5:c.5279T>A
|
ENSP00000418775.1:p.Ile1760Asn
|
|
ENST00000586385.5:c.350T>A
|
ENSP00000465818.1:p.Ile117Asn
|
|
ENST00000591534.5:c.893T>A
|
ENSP00000467329.1:p.Ile298Asn
|
|
ENST00000591849.5:c.119T>A
|
ENSP00000465347.1:p.Ile40Asn
|
|
NM_007294.3:c.5420T>A , LRG_292t1:c.5420T>A
|
NP_009225.1:p.Ile1807Asn
|
|
NM_007297.3:c.5279T>A
|
NP_009228.2:p.Ile1760Asn
|
|
NM_007298.3:c.2108T>A
|
NP_009229.2:p.Ile703Asn
|
|
NM_007299.3:c.2034T>A
|
NP_009230.2:p.Asn678Lys
|
|
NM_007300.3:c.5483T>A
|
NP_009231.2:p.Ile1828Asn
|
|
NR_027676.1:n.5556T>A
|
|
|
NM_007294.4:c.5420T>A
MANE Select
|
NP_009225.1:p.Ile1807Asn
|
|
NM_007297.4:c.5279T>A
|
NP_009228.2:p.Ile1760Asn
|
|
NM_007299.4:c.2034T>A
|
NP_009230.2:p.Asn678Lys
|
|
NM_007300.4:c.5483T>A
|
NP_009231.2:p.Ile1828Asn
|
|
NR_027676.2:n.5597T>A
|
|
|