ENST00000461574.2:c.4132G>T
|
ENSP00000417241.2:p.Val1378Phe
|
|
ENST00000470026.6:c.4132G>T
|
ENSP00000419274.2:p.Val1378Phe
|
|
ENST00000473961.6:c.4006G>T
|
ENSP00000420201.2:p.Val1336Phe
|
|
ENST00000476777.6:c.4129G>T
|
ENSP00000417554.2:p.Val1377Phe
|
|
ENST00000477152.6:c.4054G>T
|
ENSP00000419988.2:p.Val1352Phe
|
|
ENST00000478531.6:c.820G>T
|
ENSP00000420412.2:p.Val274Phe
|
|
ENST00000489037.2:c.4054G>T
|
ENSP00000420781.2:p.Val1352Phe
|
|
ENST00000493919.6:c.682G>T
|
ENSP00000418819.2:p.Val228Phe
|
|
ENST00000494123.6:c.4132G>T
|
ENSP00000419103.2:p.Val1378Phe
|
|
ENST00000497488.2:c.3244G>T
|
ENSP00000418986.2:p.Val1082Phe
|
|
ENST00000618469.2:c.4132G>T
|
ENSP00000478114.2:p.Val1378Phe
|
|
ENST00000634433.2:c.4009G>T
|
ENSP00000489431.2:p.Val1337Phe
|
|
ENST00000644379.2:c.4132G>T
|
ENSP00000496570.2:p.Val1378Phe
|
|
ENST00000644555.2:c.682G>T
|
ENSP00000494614.2:p.Val228Phe
|
|
ENST00000652672.2:c.3991G>T
|
ENSP00000498906.2:p.Val1331Phe
|
|
ENST00000484087.6:c.700G>T
|
ENSP00000419481.2:p.Val234Phe
|
|
ENST00000700182.1:c.742G>T
|
ENSP00000514849.1:p.Val248Phe
|
|
ENST00000357654.9:c.4132G>T
MANE Select
|
ENSP00000350283.3:p.Val1378Phe
|
|
ENST00000471181.7:c.4132G>T
|
ENSP00000418960.2:p.Val1378Phe
|
|
ENST00000644379.1:c.453G>T
|
|
|
ENST00000352993.7:c.706G>T
|
ENSP00000312236.5:p.Val236Phe
|
|
ENST00000357654.7:c.4132G>T
|
ENSP00000350283.3:p.Val1378Phe
|
|
ENST00000461221.5:c.*3915G>T
|
ENSP00000418548.1:n.*3915G>T
|
|
ENST00000461574.1:c.426G>T
|
|
|
ENST00000468300.5:c.823G>T
|
ENSP00000417148.1:p.Val275Phe
|
|
ENST00000471181.6:c.4132G>T
|
ENSP00000418960.2:p.Val1378Phe
|
|
ENST00000478531.5:c.820G>T
|
ENSP00000420412.1:p.Val274Phe
|
|
ENST00000484087.5:c.445G>T
|
ENSP00000419481.1:p.Val149Phe
|
|
ENST00000487825.5:c.448G>T
|
ENSP00000418212.1:p.Val150Phe
|
|
ENST00000491747.6:c.823G>T
|
ENSP00000420705.2:p.Val275Phe
|
|
ENST00000493795.5:c.3991G>T
|
ENSP00000418775.1:p.Val1331Phe
|
|
ENST00000493919.5:c.682G>T
|
ENSP00000418819.1:p.Val228Phe
|
|
ENST00000586385.5:c.5-27046G>T
|
ENSP00000465818.1:n.5-27046G>T
|
|
ENST00000591534.5:c.-43-16476G>T
|
ENSP00000467329.1:n.-43-16476G>T
|
|
ENST00000591849.5:c.-99+34274G>T
|
ENSP00000465347.1:n.-99+34274G>T
|
|
NM_007294.3:c.4132G>T , LRG_292t1:c.4132G>T
|
NP_009225.1:p.Val1378Phe
|
|
NM_007297.3:c.3991G>T
|
NP_009228.2:p.Val1331Phe
|
|
NM_007298.3:c.823G>T
|
NP_009229.2:p.Val275Phe
|
|
NM_007299.3:c.823G>T
|
NP_009230.2:p.Val275Phe
|
|
NM_007300.3:c.4132G>T
|
NP_009231.2:p.Val1378Phe
|
|
NR_027676.1:n.4268G>T
|
|
|
NM_007294.4:c.4132G>T
MANE Select
|
NP_009225.1:p.Val1378Phe
|
|
NM_007297.4:c.3991G>T
|
NP_009228.2:p.Val1331Phe
|
|
NM_007299.4:c.823G>T
|
NP_009230.2:p.Val275Phe
|
|
NM_007300.4:c.4132G>T
|
NP_009231.2:p.Val1378Phe
|
|
NR_027676.2:n.4309G>T
|
|
|