|
ENST00000529510.6:n.1328C>T
(SLC37A4)
|
|
|
|
ENST00000697845.1:n.2317C>T
(SLC37A4)
|
|
|
|
ENST00000697846.1:n.1690C>T
(SLC37A4)
|
|
|
|
ENST00000697847.1:n.1401C>T
(SLC37A4)
|
|
|
|
ENST00000697849.1:n.3794C>T
(SLC37A4)
|
|
|
|
ENST00000697850.1:n.1985C>T
(SLC37A4)
|
|
|
|
ENST00000697851.1:n.2956C>T
(SLC37A4)
|
|
|
|
ENST00000638186.1:n.1422C>T
(SLC37A4)
|
|
|
|
ENST00000638360.1:n.1254C>T
(SLC37A4)
|
|
|
|
ENST00000638925.1:n.1387C>T
(SLC37A4)
|
|
|
|
ENST00000650539.1:n.1590C>T
(SLC37A4)
|
|
|
|
ENST00000330775.9:c.1118C>T
(SLC37A4)
|
ENSP00000476242.2:p.Ala373Val
|
|
|
ENST00000357590.9:c.1184C>T
(SLC37A4)
|
ENSP00000476176.2:p.Ala395Val
|
|
|
ENST00000524428.5:n.1354C>T
(SLC37A4)
|
|
|
|
ENST00000525039.5:n.1608C>T
(SLC37A4)
|
|
|
|
ENST00000525102.5:n.1876C>T
(SLC37A4)
|
|
|
|
ENST00000525372.5:n.1216C>T
(SLC37A4)
|
|
|
|
ENST00000526275.5:n.1900C>T
(SLC37A4)
|
|
|
|
ENST00000527992.5:n.1346C>T
(SLC37A4)
|
|
|
|
ENST00000529510.5:n.806C>T
(SLC37A4)
|
|
|
|
ENST00000530407.5:n.1268C>T
(SLC37A4)
|
|
|
|
ENST00000532085.1:n.5136C>T
(SLC37A4)
|
|
|
|
ENST00000533058.5:c.*147G>A
(TRAPPC4)
|
ENSP00000432920.1:n.*147G>A
|
|
|
ENST00000538950.5:c.899C>T
(SLC37A4)
|
ENSP00000475991.2:p.Ala300Val
|
|
|
ENST00000545985.5:c.1118C>T
(SLC37A4)
|
ENSP00000475241.2:p.Ala373Val
|
|
|
NM_001164277.1:c.1118C>T , LRG_187t1:c.1118C>T
(SLC37A4)
|
NP_001157749.1:p.Ala373Val
|
|
|
NM_001164278.1:c.1184C>T
(SLC37A4)
|
NP_001157750.1:p.Ala395Val
|
|
|
NM_001164279.1:c.899C>T
(SLC37A4)
|
NP_001157751.1:p.Ala300Val
|
|
|
NM_001164280.1:c.1118C>T
(SLC37A4)
|
NP_001157752.1:p.Ala373Val
|
|
|
NM_001467.5:c.1118C>T
(SLC37A4)
|
NP_001458.1:p.Ala373Val
|
|
|
NM_001164278.2:c.1184C>T
(SLC37A4)
|
NP_001157750.1:p.Ala395Val
|
|
|
NM_001164279.2:c.899C>T
(SLC37A4)
|
NP_001157751.1:p.Ala300Val
|
|
|
NM_001164280.2:c.1118C>T
(SLC37A4)
|
NP_001157752.1:p.Ala373Val
|
|
|
NM_001467.6:c.1118C>T
(SLC37A4)
|
NP_001458.1:p.Ala373Val
|
|
|
NM_001164277.2:c.1118C>T
(SLC37A4)
MANE Select
|
NP_001157749.1:p.Ala373Val
|
|
