|
ENST00000222214.10:c.1317A=
(GCDH)
MANE Select
|
ENSP00000222214.4:p.Ter439=
|
|
|
ENST00000293695.8:c.613-156T=
(SYCE2)
MANE Select
|
ENSP00000293695.6:n.613-156T=
|
|
|
ENST00000222214.9:c.1317A=
(GCDH)
|
ENSP00000222214.4:p.Ter439=
|
|
|
ENST00000293695.7:c.613-156T=
(SYCE2)
|
ENSP00000293695.6:n.613-156T=
|
|
|
ENST00000585420.5:n.1647A=
(GCDH)
|
|
|
|
ENST00000590530.5:c.*757A=
(GCDH)
|
ENSP00000468452.1:n.*757A=
|
|
|
ENST00000591043.1:n.1627A=
(GCDH)
|
|
|
|
ENST00000591050.1:c.210+1678A=
(GCDH)
|
|
|
|
ENST00000591470.5:c.1317A=
(GCDH)
|
ENSP00000466845.1:p.Ter439=
|
|
|
ENST00000592819.1:c.186-156T=
(SYCE2)
|
|
|
|
NM_000159.3:c.1317A=
(GCDH)
|
NP_000150.1:p.Ter439=
|
|
|
NM_001105578.1:c.613-156T=
(SYCE2)
|
NP_001099048.1:n.613-156T=
|
|
|
NM_013976.3:c.1244-159A=
(GCDH)
|
NP_039663.1:n.1244-159A=
|
|
|
NR_102316.1:n.1480A=
(GCDH)
|
|
|
|
NR_102317.1:n.1698A=
(GCDH)
|
|
|
|
XM_005259848.3:c.*23-156T=
(SYCE2)
|
XP_005259905.1:n.*23-156T=
|
|
|
XM_006722721.2:c.1244-693A=
(GCDH)
|
XP_006722784.1:n.1244-693A=
|
|
|
XM_011527882.1:c.610-156T=
(SYCE2)
|
XP_011526184.1:n.610-156T=
|
|
|
XM_011527883.1:c.*23-156T=
(SYCE2)
|
XP_011526185.1:n.*23-156T=
|
|
|
XM_011527899.1:c.1243+1678A=
(GCDH)
|
XP_011526201.1:n.1243+1678A=
|
|
|
XM_011527900.1:c.1244-693A=
(GCDH)
|
XP_011526202.1:n.1244-693A=
|
|
|
XM_005259848.4:c.*23-156T=
(SYCE2)
|
XP_005259905.1:n.*23-156T=
|
|
|
XM_011527882.2:c.610-156T=
(SYCE2)
|
XP_011526184.1:n.610-156T=
|
|
|
XM_011527883.2:c.*23-156T=
(SYCE2)
|
XP_011526185.1:n.*23-156T=
|
|
|
XM_011527899.2:c.1243+1678A=
(GCDH)
|
XP_011526201.1:n.1243+1678A=
|
|
|
XM_011527900.2:c.1244-693A=
(GCDH)
|
XP_011526202.1:n.1244-693A=
|
|
|
XM_017026580.1:c.1244-693A=
(GCDH)
|
XP_016882069.1:n.1244-693A=
|
|
|
NM_000159.4:c.1317A=
(GCDH)
MANE Select
|
NP_000150.1:p.Ter439=
|
|
|
NM_001105578.2:c.613-156T=
(SYCE2)
MANE Select
|
NP_001099048.1:n.613-156T=
|
|
|
NM_013976.4:c.1244-159A=
(GCDH)
|
NP_039663.1:n.1244-159A=
|
|
|
NM_013976.5:c.1244-159A=
(GCDH)
|
NP_039663.1:n.1244-159A=
|
|
