|
ENST00000529510.6:n.1210T>G
(SLC37A4)
|
|
|
|
ENST00000697845.1:n.2199T>G
(SLC37A4)
|
|
|
|
ENST00000697846.1:n.1572T>G
(SLC37A4)
|
|
|
|
ENST00000697847.1:n.1283T>G
(SLC37A4)
|
|
|
|
ENST00000697849.1:n.3676T>G
(SLC37A4)
|
|
|
|
ENST00000697850.1:n.1867T>G
(SLC37A4)
|
|
|
|
ENST00000697851.1:n.2838T>G
(SLC37A4)
|
|
|
|
ENST00000638186.1:n.1304T>G
(SLC37A4)
|
|
|
|
ENST00000638360.1:n.1136T>G
(SLC37A4)
|
|
|
|
ENST00000638925.1:n.1269T>G
(SLC37A4)
|
|
|
|
ENST00000650539.1:n.1472T>G
(SLC37A4)
|
|
|
|
ENST00000330775.9:c.1000T>G
(SLC37A4)
|
ENSP00000476242.2:p.Leu334Val
|
|
|
ENST00000357590.9:c.1066T>G
(SLC37A4)
|
ENSP00000476176.2:p.Leu356Val
|
|
|
ENST00000524428.5:n.1236T>G
(SLC37A4)
|
|
|
|
ENST00000525039.5:n.1490T>G
(SLC37A4)
|
|
|
|
ENST00000525102.5:n.1758T>G
(SLC37A4)
|
|
|
|
ENST00000525372.5:n.1098T>G
(SLC37A4)
|
|
|
|
ENST00000526275.5:n.1782T>G
(SLC37A4)
|
|
|
|
ENST00000527992.5:n.1228T>G
(SLC37A4)
|
|
|
|
ENST00000529510.5:n.688T>G
(SLC37A4)
|
|
|
|
ENST00000530407.5:n.1150T>G
(SLC37A4)
|
|
|
|
ENST00000532085.1:n.5018T>G
(SLC37A4)
|
|
|
|
ENST00000533058.5:c.*265A>C
(TRAPPC4)
|
ENSP00000432920.1:n.*265A>C
|
|
|
ENST00000538950.5:c.781T>G
(SLC37A4)
|
ENSP00000475991.2:p.Leu261Val
|
|
|
ENST00000545985.5:c.1000T>G
(SLC37A4)
|
ENSP00000475241.2:p.Leu334Val
|
|
|
NM_001164277.1:c.1000T>G , LRG_187t1:c.1000T>G
(SLC37A4)
|
NP_001157749.1:p.Leu334Val
|
|
|
NM_001164278.1:c.1066T>G
(SLC37A4)
|
NP_001157750.1:p.Leu356Val
|
|
|
NM_001164279.1:c.781T>G
(SLC37A4)
|
NP_001157751.1:p.Leu261Val
|
|
|
NM_001164280.1:c.1000T>G
(SLC37A4)
|
NP_001157752.1:p.Leu334Val
|
|
|
NM_001467.5:c.1000T>G
(SLC37A4)
|
NP_001458.1:p.Leu334Val
|
|
|
NM_001164278.2:c.1066T>G
(SLC37A4)
|
NP_001157750.1:p.Leu356Val
|
|
|
NM_001164279.2:c.781T>G
(SLC37A4)
|
NP_001157751.1:p.Leu261Val
|
|
|
NM_001164280.2:c.1000T>G
(SLC37A4)
|
NP_001157752.1:p.Leu334Val
|
|
|
NM_001467.6:c.1000T>G
(SLC37A4)
|
NP_001458.1:p.Leu334Val
|
|
|
NM_001164277.2:c.1000T>G
(SLC37A4)
MANE Select
|
NP_001157749.1:p.Leu334Val
|
|
