ENST00000292408.9:c.527G>A
MANE Select
|
ENSP00000292408.4:p.Gly176Asp
|
|
ENST00000292408.8:c.527G>A
|
ENSP00000292408.4:p.Gly176Asp
|
|
ENST00000393637.5:c.527G>A
|
ENSP00000377254.1:p.Gly176Asp
|
|
ENST00000393648.6:c.527G>A
|
ENSP00000377259.2:p.Gly176Asp
|
|
ENST00000426612.5:n.644G>A
|
|
|
ENST00000430285.5:c.*391G>A
|
ENSP00000395164.1:n.*391G>A
|
|
ENST00000502906.5:c.527G>A
|
ENSP00000424960.1:p.Gly176Asp
|
|
ENST00000503708.5:c.527G>A
|
ENSP00000424905.1:p.Gly176Asp
|
|
ENST00000509511.5:n.527G>A
|
|
|
NM_001291980.1:c.527G>A
|
NP_001278909.1:p.Gly176Asp
|
|
NM_002011.4:c.527G>A
|
NP_002002.3:p.Gly176Asp
|
|
NM_022963.3:c.527G>A
|
NP_075252.2:p.Gly176Asp
|
|
NM_213647.2:c.527G>A
|
NP_998812.1:p.Gly176Asp
|
|
XM_005265838.2:c.527G>A
|
XP_005265895.1:p.Gly176Asp
|
|
XM_011534464.1:c.620G>A
|
XP_011532766.1:p.Gly207Asp
|
|
XM_011534465.1:c.209G>A
|
XP_011532767.1:p.Gly70Asp
|
|
XR_941090.1:n.572G>A
|
|
|
NM_001354984.1:c.527G>A
|
NP_001341913.1:p.Gly176Asp
|
|
NM_213647.3:c.527G>A
MANE Select
|
NP_998812.1:p.Gly176Asp
|
|
NM_001291980.2:c.527G>A
|
NP_001278909.1:p.Gly176Asp
|
|
NM_001354984.2:c.527G>A
|
NP_001341913.1:p.Gly176Asp
|
|
NM_002011.5:c.527G>A
|
NP_002002.3:p.Gly176Asp
|
|