ENST00000328300.11:c.4925G>A
MANE Select
|
ENSP00000331902.7:p.Gly1642Asp
|
|
ENST00000361603.7:c.4907G>A
|
ENSP00000354505.2:p.Gly1636Asp
|
|
ENST00000510690.2:n.1419G>A
|
|
|
ENST00000644079.1:n.1756G>A
|
|
|
ENST00000328300.10:c.4925G>A
|
ENSP00000331902.6:p.Gly1642Asp
|
|
ENST00000361603.6:c.4907G>A
|
ENSP00000354505.2:p.Gly1636Asp
|
|
ENST00000504541.1:c.219+449G>A
|
ENSP00000424845.1:n.219+449G>A
|
|
ENST00000515658.1:c.325-927G>A
|
|
|
NM_000495.4:c.4907G>A
|
NP_000486.1:p.Gly1636Asp
|
|
NM_033380.2:c.4925G>A
|
NP_203699.1:p.Gly1642Asp
|
|
XM_005262070.2:c.4916G>A
|
XP_005262127.1:p.Gly1639Asp
|
|
XM_006724616.2:c.4925G>A
|
XP_006724679.1:p.Gly1642Asp
|
|
XM_011530849.1:c.4601G>A
|
XP_011529151.1:p.Gly1534Asp
|
|
XM_011530851.1:c.2498G>A
|
XP_011529153.1:p.Gly833Asp
|
|
XM_011530849.2:c.4940G>A
|
XP_011529151.2:p.Gly1647Asp
|
|
XM_017029259.2:c.4931G>A
|
XP_016884748.1:p.Gly1644Asp
|
|
XM_017029260.1:c.4922G>A
|
XP_016884749.1:p.Gly1641Asp
|
|
XM_017029263.2:c.3260G>A
|
XP_016884752.1:p.Gly1087Asp
|
|
NM_000495.5:c.4907G>A
|
NP_000486.1:p.Gly1636Asp
|
|
NM_033380.3:c.4925G>A
MANE Select
|
NP_203699.1:p.Gly1642Asp
|
|