ENST00000296805.8:c.2253T>G
(GFM2)
MANE Select
|
ENSP00000296805.3:p.Ala751=
|
|
ENST00000296805.7:c.2253T>G
(GFM2)
|
ENSP00000296805.3:p.Ala751=
|
|
ENST00000345239.6:c.2112T>G
(GFM2)
|
ENSP00000296804.3:p.Ala704=
|
|
ENST00000503312.5:c.608+306A>C
(HEXB)
|
|
|
ENST00000505859.1:c.255+306A>C
(HEXB)
|
|
|
ENST00000509430.5:c.2253T>G
(GFM2)
|
ENSP00000427004.1:p.Ala751=
|
|
ENST00000513867.1:n.380+306A>C
(HEXB)
|
|
|
ENST00000515125.5:n.656T>G
(GFM2)
|
|
|
NM_001281302.1:c.2349T>G
(GFM2)
|
NP_001268231.1:p.Ala783=
|
|
NM_032380.4:c.2253T>G
(GFM2)
|
NP_115756.2:p.Ala751=
|
|
NM_170691.2:c.2112T>G
(GFM2)
|
NP_733792.1:p.Ala704=
|
|
NR_104006.1:n.2572T>G
(GFM2)
|
|
|
XM_006714721.2:c.2118T>G
(GFM2)
|
XP_006714784.1:p.Ala706=
|
|
XM_011543690.1:c.2253T>G
(GFM2)
|
XP_011541992.1:p.Ala751=
|
|
XM_017009986.1:c.2253T>G
(GFM2)
|
XP_016865475.1:p.Ala751=
|
|
XR_002956185.1:n.3539T>G
(GFM2)
|
|
|
NM_032380.5:c.2253T>G
(GFM2)
MANE Select
|
NP_115756.2:p.Ala751=
|
|
NM_001281302.2:c.2349T>G
(GFM2)
|
NP_001268231.1:p.Ala783=
|
|
NM_170691.3:c.2112T>G
(GFM2)
|
NP_733792.1:p.Ala704=
|
|
NR_104006.2:n.2318T>G
(GFM2)
|
|
|