ENST00000461574.2:c.5303A>T
|
ENSP00000417241.2:p.Tyr1768Phe
|
|
ENST00000470026.6:c.5306A>T
|
ENSP00000419274.2:p.Tyr1769Phe
|
|
ENST00000473961.6:c.5180A>T
|
ENSP00000420201.2:p.Tyr1727Phe
|
|
ENST00000476777.6:c.5300A>T
|
ENSP00000417554.2:p.Tyr1767Phe
|
|
ENST00000477152.6:c.5228A>T
|
ENSP00000419988.2:p.Tyr1743Phe
|
|
ENST00000478531.6:c.1994A>T
|
ENSP00000420412.2:p.Tyr665Phe
|
|
ENST00000489037.2:c.5228A>T
|
ENSP00000420781.2:p.Tyr1743Phe
|
|
ENST00000493919.6:c.1856A>T
|
ENSP00000418819.2:p.Tyr619Phe
|
|
ENST00000494123.6:c.5306A>T
|
ENSP00000419103.2:p.Tyr1769Phe
|
|
ENST00000497488.2:c.4418A>T
|
ENSP00000418986.2:p.Tyr1473Phe
|
|
ENST00000618469.2:c.5306A>T
|
ENSP00000478114.2:p.Tyr1769Phe
|
|
ENST00000634433.2:c.5183A>T
|
ENSP00000489431.2:p.Tyr1728Phe
|
|
ENST00000644379.2:c.5372A>T
|
ENSP00000496570.2:p.Tyr1791Phe
|
|
ENST00000644555.2:c.1856A>T
|
ENSP00000494614.2:p.Tyr619Phe
|
|
ENST00000652672.2:c.5165A>T
|
ENSP00000498906.2:p.Tyr1722Phe
|
|
ENST00000484087.6:c.1868A>T
|
ENSP00000419481.2:p.Tyr623Phe
|
|
ENST00000357654.9:c.5306A>T
MANE Select
|
ENSP00000350283.3:p.Tyr1769Phe
|
|
ENST00000471181.7:c.5369A>T
|
ENSP00000418960.2:p.Tyr1790Phe
|
|
ENST00000644379.1:c.1693A>T
|
|
|
ENST00000352993.7:c.1880A>T
|
ENSP00000312236.5:p.Tyr627Phe
|
|
ENST00000357654.7:c.5306A>T
|
ENSP00000350283.3:p.Tyr1769Phe
|
|
ENST00000461221.5:c.*5089A>T
|
ENSP00000418548.1:n.*5089A>T
|
|
ENST00000468300.5:c.1994A>T
|
ENSP00000417148.1:p.Tyr665Phe
|
|
ENST00000471181.6:c.5369A>T
|
ENSP00000418960.2:p.Tyr1790Phe
|
|
ENST00000491747.6:c.1994A>T
|
ENSP00000420705.2:p.Tyr665Phe
|
|
ENST00000493795.5:c.5165A>T
|
ENSP00000418775.1:p.Tyr1722Phe
|
|
ENST00000586385.5:c.236A>T
|
ENSP00000465818.1:p.Tyr79Phe
|
|
ENST00000591534.5:c.779A>T
|
ENSP00000467329.1:p.Tyr260Phe
|
|
ENST00000591849.5:c.-98-899A>T
|
ENSP00000465347.1:n.-98-899A>T
|
|
NM_007294.3:c.5306A>T , LRG_292t1:c.5306A>T
|
NP_009225.1:p.Tyr1769Phe
|
|
NM_007297.3:c.5165A>T
|
NP_009228.2:p.Tyr1722Phe
|
|
NM_007298.3:c.1994A>T
|
NP_009229.2:p.Tyr665Phe
|
|
NM_007299.3:c.1994A>T
|
NP_009230.2:p.Tyr665Phe
|
|
NM_007300.3:c.5369A>T
|
NP_009231.2:p.Tyr1790Phe
|
|
NR_027676.1:n.5442A>T
|
|
|
NM_007294.4:c.5306A>T
MANE Select
|
NP_009225.1:p.Tyr1769Phe
|
|
NM_007297.4:c.5165A>T
|
NP_009228.2:p.Tyr1722Phe
|
|
NM_007299.4:c.1994A>T
|
NP_009230.2:p.Tyr665Phe
|
|
NM_007300.4:c.5369A>T
|
NP_009231.2:p.Tyr1790Phe
|
|
NR_027676.2:n.5483A>T
|
|
|