ENST00000296805.8:c.2262C>G
(GFM2)
MANE Select
|
ENSP00000296805.3:p.Ala754=
|
|
ENST00000296805.7:c.2262C>G
(GFM2)
|
ENSP00000296805.3:p.Ala754=
|
|
ENST00000345239.6:c.2121C>G
(GFM2)
|
ENSP00000296804.3:p.Ala707=
|
|
ENST00000503312.5:c.608+297G>C
(HEXB)
|
|
|
ENST00000505859.1:c.255+297G>C
(HEXB)
|
|
|
ENST00000509430.5:c.2262C>G
(GFM2)
|
ENSP00000427004.1:p.Ala754=
|
|
ENST00000513867.1:n.380+297G>C
(HEXB)
|
|
|
ENST00000515125.5:n.665C>G
(GFM2)
|
|
|
NM_001281302.1:c.2358C>G
(GFM2)
|
NP_001268231.1:p.Ala786=
|
|
NM_032380.4:c.2262C>G
(GFM2)
|
NP_115756.2:p.Ala754=
|
|
NM_170691.2:c.2121C>G
(GFM2)
|
NP_733792.1:p.Ala707=
|
|
NR_104006.1:n.2581C>G
(GFM2)
|
|
|
XM_006714721.2:c.2127C>G
(GFM2)
|
XP_006714784.1:p.Ala709=
|
|
XM_011543690.1:c.2262C>G
(GFM2)
|
XP_011541992.1:p.Ala754=
|
|
XM_017009986.1:c.2262C>G
(GFM2)
|
XP_016865475.1:p.Ala754=
|
|
XR_002956185.1:n.3548C>G
(GFM2)
|
|
|
NM_032380.5:c.2262C>G
(GFM2)
MANE Select
|
NP_115756.2:p.Ala754=
|
|
NM_001281302.2:c.2358C>G
(GFM2)
|
NP_001268231.1:p.Ala786=
|
|
NM_170691.3:c.2121C>G
(GFM2)
|
NP_733792.1:p.Ala707=
|
|
NR_104006.2:n.2327C>G
(GFM2)
|
|
|