ENST00000461574.2:c.5253A>G
|
ENSP00000417241.2:p.Ala1751=
|
|
ENST00000470026.6:c.5256A>G
|
ENSP00000419274.2:p.Ala1752=
|
|
ENST00000473961.6:c.5130A>G
|
ENSP00000420201.2:p.Ala1710=
|
|
ENST00000476777.6:c.5250A>G
|
ENSP00000417554.2:p.Ala1750=
|
|
ENST00000477152.6:c.5178A>G
|
ENSP00000419988.2:p.Ala1726=
|
|
ENST00000478531.6:c.1944A>G
|
ENSP00000420412.2:p.Ala648=
|
|
ENST00000489037.2:c.5178A>G
|
ENSP00000420781.2:p.Ala1726=
|
|
ENST00000493919.6:c.1806A>G
|
ENSP00000418819.2:p.Ala602=
|
|
ENST00000494123.6:c.5256A>G
|
ENSP00000419103.2:p.Ala1752=
|
|
ENST00000497488.2:c.4368A>G
|
ENSP00000418986.2:p.Ala1456=
|
|
ENST00000618469.2:c.5256A>G
|
ENSP00000478114.2:p.Ala1752=
|
|
ENST00000634433.2:c.5133A>G
|
ENSP00000489431.2:p.Ala1711=
|
|
ENST00000644379.2:c.5322A>G
|
ENSP00000496570.2:p.Ala1774=
|
|
ENST00000644555.2:c.1806A>G
|
ENSP00000494614.2:p.Ala602=
|
|
ENST00000652672.2:c.5115A>G
|
ENSP00000498906.2:p.Ala1705=
|
|
ENST00000484087.6:c.1818A>G
|
ENSP00000419481.2:p.Ala606=
|
|
ENST00000357654.9:c.5256A>G
MANE Select
|
ENSP00000350283.3:p.Ala1752=
|
|
ENST00000471181.7:c.5319A>G
|
ENSP00000418960.2:p.Ala1773=
|
|
ENST00000644379.1:c.1643A>G
|
|
|
ENST00000352993.7:c.1830A>G
|
ENSP00000312236.5:p.Ala610=
|
|
ENST00000357654.7:c.5256A>G
|
ENSP00000350283.3:p.Ala1752=
|
|
ENST00000461221.5:c.*5039A>G
|
ENSP00000418548.1:n.*5039A>G
|
|
ENST00000468300.5:c.1944A>G
|
ENSP00000417148.1:p.Ala648=
|
|
ENST00000471181.6:c.5319A>G
|
ENSP00000418960.2:p.Ala1773=
|
|
ENST00000491747.6:c.1944A>G
|
ENSP00000420705.2:p.Ala648=
|
|
ENST00000493795.5:c.5115A>G
|
ENSP00000418775.1:p.Ala1705=
|
|
ENST00000586385.5:c.186A>G
|
ENSP00000465818.1:p.Ala62=
|
|
ENST00000591534.5:c.729A>G
|
ENSP00000467329.1:p.Ala243=
|
|
ENST00000591849.5:c.-98-6883A>G
|
ENSP00000465347.1:n.-98-6883A>G
|
|
NM_007294.3:c.5256A>G , LRG_292t1:c.5256A>G
|
NP_009225.1:p.Ala1752=
|
|
NM_007297.3:c.5115A>G
|
NP_009228.2:p.Ala1705=
|
|
NM_007298.3:c.1944A>G
|
NP_009229.2:p.Ala648=
|
|
NM_007299.3:c.1944A>G
|
NP_009230.2:p.Ala648=
|
|
NM_007300.3:c.5319A>G
|
NP_009231.2:p.Ala1773=
|
|
NR_027676.1:n.5392A>G
|
|
|
NM_007294.4:c.5256A>G
MANE Select
|
NP_009225.1:p.Ala1752=
|
|
NM_007297.4:c.5115A>G
|
NP_009228.2:p.Ala1705=
|
|
NM_007299.4:c.1944A>G
|
NP_009230.2:p.Ala648=
|
|
NM_007300.4:c.5319A>G
|
NP_009231.2:p.Ala1773=
|
|
NR_027676.2:n.5433A>G
|
|
|