|
ENST00000354071.8:n.4159A>T
|
|
|
|
ENST00000461574.2:c.4095A>T
|
ENSP00000417241.2:p.Leu1365Phe
|
|
|
ENST00000470026.6:c.4095A>T
|
ENSP00000419274.2:p.Leu1365Phe
|
|
|
ENST00000473961.6:c.3969A>T
|
ENSP00000420201.2:p.Leu1323Phe
|
|
|
ENST00000476777.6:c.4092A>T
|
ENSP00000417554.2:p.Leu1364Phe
|
|
|
ENST00000477152.6:c.4017A>T
|
ENSP00000419988.2:p.Leu1339Phe
|
|
|
ENST00000478531.6:c.785-404A>T
|
ENSP00000420412.2:n.785-404A>T
|
|
|
ENST00000489037.2:c.4017A>T
|
ENSP00000420781.2:p.Leu1339Phe
|
|
|
ENST00000493919.6:c.647-404A>T
|
ENSP00000418819.2:n.647-404A>T
|
|
|
ENST00000494123.6:c.4095A>T
|
ENSP00000419103.2:p.Leu1365Phe
|
|
|
ENST00000497488.2:c.3207A>T
|
ENSP00000418986.2:p.Leu1069Phe
|
|
|
ENST00000618469.2:c.4095A>T
|
ENSP00000478114.2:p.Leu1365Phe
|
|
|
ENST00000634433.2:c.3972A>T
|
ENSP00000489431.2:p.Leu1324Phe
|
|
|
ENST00000644379.2:c.4095A>T
|
ENSP00000496570.2:p.Leu1365Phe
|
|
|
ENST00000644555.2:c.647-404A>T
|
ENSP00000494614.2:n.647-404A>T
|
|
|
ENST00000652672.2:c.3954A>T
|
ENSP00000498906.2:p.Leu1318Phe
|
|
|
ENST00000484087.6:c.665-404A>T
|
ENSP00000419481.2:n.665-404A>T
|
|
|
ENST00000700182.1:c.707-404A>T
|
ENSP00000514849.1:n.707-404A>T
|
|
|
ENST00000357654.9:c.4095A>T
MANE Select
|
ENSP00000350283.3:p.Leu1365Phe
|
|
|
ENST00000471181.7:c.4095A>T
|
ENSP00000418960.2:p.Leu1365Phe
|
|
|
ENST00000644379.1:c.416A>T
|
|
|
|
ENST00000352993.7:c.671-404A>T
|
ENSP00000312236.5:n.671-404A>T
|
|
|
ENST00000354071.7:c.4095A>T
|
ENSP00000326002.7:p.Leu1365Phe
|
|
|
ENST00000357654.7:c.4095A>T
|
ENSP00000350283.3:p.Leu1365Phe
|
|
|
ENST00000461221.5:c.*3878A>T
|
ENSP00000418548.1:n.*3878A>T
|
|
|
ENST00000461574.1:c.389A>T
|
|
|
|
ENST00000468300.5:c.788-404A>T
|
ENSP00000417148.1:n.788-404A>T
|
|
|
ENST00000471181.6:c.4095A>T
|
ENSP00000418960.2:p.Leu1365Phe
|
|
|
ENST00000478531.5:c.785-404A>T
|
ENSP00000420412.1:n.785-404A>T
|
|
|
ENST00000484087.5:c.410-404A>T
|
ENSP00000419481.1:n.410-404A>T
|
|
|
ENST00000487825.5:c.413-404A>T
|
ENSP00000418212.1:n.413-404A>T
|
|
|
ENST00000491747.6:c.788-404A>T
|
ENSP00000420705.2:n.788-404A>T
|
|
|
ENST00000493795.5:c.3954A>T
|
ENSP00000418775.1:p.Leu1318Phe
|
|
|
ENST00000493919.5:c.647-404A>T
|
ENSP00000418819.1:n.647-404A>T
|
|
|
ENST00000586385.5:c.5-27485A>T
|
ENSP00000465818.1:n.5-27485A>T
|
|
|
ENST00000591534.5:c.-43-16915A>T
|
ENSP00000467329.1:n.-43-16915A>T
|
|
|
ENST00000591849.5:c.-99+33835A>T
|
ENSP00000465347.1:n.-99+33835A>T
|
|
|
NM_007294.3:c.4095A>T , LRG_292t1:c.4095A>T
|
NP_009225.1:p.Leu1365Phe
|
|
|
NM_007297.3:c.3954A>T
|
NP_009228.2:p.Leu1318Phe
|
|
|
NM_007298.3:c.788-404A>T
|
NP_009229.2:n.788-404A>T
|
|
|
NM_007299.3:c.788-404A>T
|
NP_009230.2:n.788-404A>T
|
|
|
NM_007300.3:c.4095A>T
|
NP_009231.2:p.Leu1365Phe
|
|
|
NR_027676.1:n.4231A>T
|
|
|
|
NM_007294.4:c.4095A>T
MANE Select
|
NP_009225.1:p.Leu1365Phe
|
|
|
NM_007297.4:c.3954A>T
|
NP_009228.2:p.Leu1318Phe
|
|
|
NM_007299.4:c.788-404A>T
|
NP_009230.2:n.788-404A>T
|
|
|
NM_007300.4:c.4095A>T
|
NP_009231.2:p.Leu1365Phe
|
|
|
NR_027676.2:n.4272A>T
|
|
|
