ENST00000296805.8:c.2257T>A
(GFM2)
MANE Select
|
ENSP00000296805.3:p.Phe753Ile
|
|
ENST00000296805.7:c.2257T>A
(GFM2)
|
ENSP00000296805.3:p.Phe753Ile
|
|
ENST00000345239.6:c.2116T>A
(GFM2)
|
ENSP00000296804.3:p.Phe706Ile
|
|
ENST00000503312.5:c.608+302A>T
(HEXB)
|
|
|
ENST00000505859.1:c.255+302A>T
(HEXB)
|
|
|
ENST00000509430.5:c.2257T>A
(GFM2)
|
ENSP00000427004.1:p.Phe753Ile
|
|
ENST00000513867.1:n.380+302A>T
(HEXB)
|
|
|
ENST00000515125.5:n.660T>A
(GFM2)
|
|
|
NM_001281302.1:c.2353T>A
(GFM2)
|
NP_001268231.1:p.Phe785Ile
|
|
NM_032380.4:c.2257T>A
(GFM2)
|
NP_115756.2:p.Phe753Ile
|
|
NM_170691.2:c.2116T>A
(GFM2)
|
NP_733792.1:p.Phe706Ile
|
|
NR_104006.1:n.2576T>A
(GFM2)
|
|
|
XM_006714721.2:c.2122T>A
(GFM2)
|
XP_006714784.1:p.Phe708Ile
|
|
XM_011543690.1:c.2257T>A
(GFM2)
|
XP_011541992.1:p.Phe753Ile
|
|
XM_017009986.1:c.2257T>A
(GFM2)
|
XP_016865475.1:p.Phe753Ile
|
|
XR_002956185.1:n.3543T>A
(GFM2)
|
|
|
NM_032380.5:c.2257T>A
(GFM2)
MANE Select
|
NP_115756.2:p.Phe753Ile
|
|
NM_001281302.2:c.2353T>A
(GFM2)
|
NP_001268231.1:p.Phe785Ile
|
|
NM_170691.3:c.2116T>A
(GFM2)
|
NP_733792.1:p.Phe706Ile
|
|
NR_104006.2:n.2322T>A
(GFM2)
|
|
|