ENST00000262367.10:c.4406G>A
MANE Select
|
ENSP00000262367.5:p.Gly1469Glu
|
|
ENST00000262367.9:c.4406G>A
|
ENSP00000262367.5:p.Gly1469Glu
|
|
ENST00000382070.7:c.4292G>A
|
ENSP00000371502.3:p.Gly1431Glu
|
|
ENST00000570939.2:c.3041G>A
|
ENSP00000461002.2:p.Gly1014Glu
|
|
ENST00000571763.5:n.196G>A
|
|
|
ENST00000574740.1:n.227G>A
|
|
|
ENST00000576720.1:n.3229G>A
|
|
|
NM_001079846.1:c.4292G>A
|
NP_001073315.1:p.Gly1431Glu
|
|
NM_004380.2:c.4406G>A
|
NP_004371.2:p.Gly1469Glu
|
|
XM_005255124.3:c.4361G>A
|
XP_005255181.1:p.Gly1454Glu
|
|
XM_005255125.3:c.3989G>A
|
XP_005255182.1:p.Gly1330Glu
|
|
XM_006720848.2:c.4145G>A
|
XP_006720911.1:p.Gly1382Glu
|
|
XM_011522380.1:c.4352G>A
|
XP_011520682.1:p.Gly1451Glu
|
|
XM_011522381.1:c.3653G>A
|
XP_011520683.1:p.Gly1218Glu
|
|
XM_005255124.4:c.4361G>A
|
XP_005255181.1:p.Gly1454Glu
|
|
XM_005255125.4:c.3989G>A
|
XP_005255182.1:p.Gly1330Glu
|
|
XM_006720848.3:c.4145G>A
|
XP_006720911.1:p.Gly1382Glu
|
|
XM_011522381.2:c.3653G>A
|
XP_011520683.1:p.Gly1218Glu
|
|
XM_017022944.1:c.4400G>A
|
XP_016878433.1:p.Gly1467Glu
|
|
NM_004380.3:c.4406G>A
MANE Select
|
NP_004371.2:p.Gly1469Glu
|
|