|
ENST00000529510.6:n.1496A>T
(SLC37A4)
|
|
|
|
ENST00000697845.1:n.2485A>T
(SLC37A4)
|
|
|
|
ENST00000697846.1:n.1858A>T
(SLC37A4)
|
|
|
|
ENST00000697847.1:n.1569A>T
(SLC37A4)
|
|
|
|
ENST00000697849.1:n.3962A>T
(SLC37A4)
|
|
|
|
ENST00000697850.1:n.2153A>T
(SLC37A4)
|
|
|
|
ENST00000697851.1:n.3124A>T
(SLC37A4)
|
|
|
|
ENST00000638186.1:n.1590A>T
(SLC37A4)
|
|
|
|
ENST00000638360.1:n.1422A>T
(SLC37A4)
|
|
|
|
ENST00000638925.1:n.1555A>T
(SLC37A4)
|
|
|
|
ENST00000650539.1:n.1758A>T
(SLC37A4)
|
|
|
|
ENST00000330775.9:c.1286A>T
(SLC37A4)
|
ENSP00000476242.2:p.Glu429Val
|
|
|
ENST00000357590.9:c.1352A>T
(SLC37A4)
|
ENSP00000476176.2:p.Glu451Val
|
|
|
ENST00000524428.5:n.1522A>T
(SLC37A4)
|
|
|
|
ENST00000525039.5:n.1776A>T
(SLC37A4)
|
|
|
|
ENST00000525102.5:n.2044A>T
(SLC37A4)
|
|
|
|
ENST00000525372.5:n.1384A>T
(SLC37A4)
|
|
|
|
ENST00000526275.5:n.2068A>T
(SLC37A4)
|
|
|
|
ENST00000527992.5:n.1514A>T
(SLC37A4)
|
|
|
|
ENST00000530407.5:n.1436A>T
(SLC37A4)
|
|
|
|
ENST00000532085.1:n.5304A>T
(SLC37A4)
|
|
|
|
ENST00000533058.5:c.639T>A
(TRAPPC4)
|
ENSP00000432920.1:p.Thr213=
|
|
|
ENST00000538950.5:c.1067A>T
(SLC37A4)
|
ENSP00000475991.2:p.Glu356Val
|
|
|
ENST00000545985.5:c.1286A>T
(SLC37A4)
|
ENSP00000475241.2:p.Glu429Val
|
|
|
NM_001164277.1:c.1286A>T , LRG_187t1:c.1286A>T
(SLC37A4)
|
NP_001157749.1:p.Glu429Val
|
|
|
NM_001164278.1:c.1352A>T
(SLC37A4)
|
NP_001157750.1:p.Glu451Val
|
|
|
NM_001164279.1:c.1067A>T
(SLC37A4)
|
NP_001157751.1:p.Glu356Val
|
|
|
NM_001164280.1:c.1286A>T
(SLC37A4)
|
NP_001157752.1:p.Glu429Val
|
|
|
NM_001467.5:c.1286A>T
(SLC37A4)
|
NP_001458.1:p.Glu429Val
|
|
|
NM_001164278.2:c.1352A>T
(SLC37A4)
|
NP_001157750.1:p.Glu451Val
|
|
|
NM_001164279.2:c.1067A>T
(SLC37A4)
|
NP_001157751.1:p.Glu356Val
|
|
|
NM_001164280.2:c.1286A>T
(SLC37A4)
|
NP_001157752.1:p.Glu429Val
|
|
|
NM_001467.6:c.1286A>T
(SLC37A4)
|
NP_001458.1:p.Glu429Val
|
|
|
NM_001164277.2:c.1286A>T
(SLC37A4)
MANE Select
|
NP_001157749.1:p.Glu429Val
|
|
