|
ENST00000529510.6:n.1299C>G
(SLC37A4)
|
|
|
|
ENST00000697845.1:n.2288C>G
(SLC37A4)
|
|
|
|
ENST00000697846.1:n.1661C>G
(SLC37A4)
|
|
|
|
ENST00000697847.1:n.1372C>G
(SLC37A4)
|
|
|
|
ENST00000697849.1:n.3765C>G
(SLC37A4)
|
|
|
|
ENST00000697850.1:n.1956C>G
(SLC37A4)
|
|
|
|
ENST00000697851.1:n.2927C>G
(SLC37A4)
|
|
|
|
ENST00000638186.1:n.1393C>G
(SLC37A4)
|
|
|
|
ENST00000638360.1:n.1225C>G
(SLC37A4)
|
|
|
|
ENST00000638925.1:n.1358C>G
(SLC37A4)
|
|
|
|
ENST00000650539.1:n.1561C>G
(SLC37A4)
|
|
|
|
ENST00000330775.9:c.1089C>G
(SLC37A4)
|
ENSP00000476242.2:p.Gly363=
|
|
|
ENST00000357590.9:c.1155C>G
(SLC37A4)
|
ENSP00000476176.2:p.Gly385=
|
|
|
ENST00000524428.5:n.1325C>G
(SLC37A4)
|
|
|
|
ENST00000525039.5:n.1579C>G
(SLC37A4)
|
|
|
|
ENST00000525102.5:n.1847C>G
(SLC37A4)
|
|
|
|
ENST00000525372.5:n.1187C>G
(SLC37A4)
|
|
|
|
ENST00000526275.5:n.1871C>G
(SLC37A4)
|
|
|
|
ENST00000527992.5:n.1317C>G
(SLC37A4)
|
|
|
|
ENST00000529510.5:n.777C>G
(SLC37A4)
|
|
|
|
ENST00000530407.5:n.1239C>G
(SLC37A4)
|
|
|
|
ENST00000532085.1:n.5107C>G
(SLC37A4)
|
|
|
|
ENST00000533058.5:c.*176G>C
(TRAPPC4)
|
ENSP00000432920.1:n.*176G>C
|
|
|
ENST00000538950.5:c.870C>G
(SLC37A4)
|
ENSP00000475991.2:p.Gly290=
|
|
|
ENST00000545985.5:c.1089C>G
(SLC37A4)
|
ENSP00000475241.2:p.Gly363=
|
|
|
NM_001164277.1:c.1089C>G , LRG_187t1:c.1089C>G
(SLC37A4)
|
NP_001157749.1:p.Gly363=
|
|
|
NM_001164278.1:c.1155C>G
(SLC37A4)
|
NP_001157750.1:p.Gly385=
|
|
|
NM_001164279.1:c.870C>G
(SLC37A4)
|
NP_001157751.1:p.Gly290=
|
|
|
NM_001164280.1:c.1089C>G
(SLC37A4)
|
NP_001157752.1:p.Gly363=
|
|
|
NM_001467.5:c.1089C>G
(SLC37A4)
|
NP_001458.1:p.Gly363=
|
|
|
NM_001164278.2:c.1155C>G
(SLC37A4)
|
NP_001157750.1:p.Gly385=
|
|
|
NM_001164279.2:c.870C>G
(SLC37A4)
|
NP_001157751.1:p.Gly290=
|
|
|
NM_001164280.2:c.1089C>G
(SLC37A4)
|
NP_001157752.1:p.Gly363=
|
|
|
NM_001467.6:c.1089C>G
(SLC37A4)
|
NP_001458.1:p.Gly363=
|
|
|
NM_001164277.2:c.1089C>G
(SLC37A4)
MANE Select
|
NP_001157749.1:p.Gly363=
|
|
