ENST00000328300.11:c.4977T=
MANE Select
|
ENSP00000331902.7:p.Asp1659=
|
|
ENST00000361603.7:c.4959T=
|
ENSP00000354505.2:p.Asp1653=
|
|
ENST00000510690.2:n.1471T=
|
|
|
ENST00000644079.1:n.1808T=
|
|
|
ENST00000328300.10:c.4977T=
|
ENSP00000331902.6:p.Asp1659=
|
|
ENST00000361603.6:c.4959T=
|
ENSP00000354505.2:p.Asp1653=
|
|
ENST00000504541.1:c.219+501T=
|
ENSP00000424845.1:n.219+501T=
|
|
ENST00000515658.1:c.325-875T=
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|
|
NM_000495.4:c.4959T=
|
NP_000486.1:p.Asp1653=
|
|
NM_033380.2:c.4977T=
|
NP_203699.1:p.Asp1659=
|
|
XM_005262070.2:c.4968T=
|
XP_005262127.1:p.Asp1656=
|
|
XM_006724616.2:c.4977T=
|
XP_006724679.1:p.Asp1659=
|
|
XM_011530849.1:c.4653T=
|
XP_011529151.1:p.Asp1551=
|
|
XM_011530851.1:c.2550T=
|
XP_011529153.1:p.Asp850=
|
|
XM_011530849.2:c.4992T=
|
XP_011529151.2:p.Asp1664=
|
|
XM_017029259.2:c.4983T=
|
XP_016884748.1:p.Asp1661=
|
|
XM_017029260.1:c.4974T=
|
XP_016884749.1:p.Asp1658=
|
|
XM_017029263.2:c.3312T=
|
XP_016884752.1:p.Asp1104=
|
|
NM_000495.5:c.4959T=
|
NP_000486.1:p.Asp1653=
|
|
NM_033380.3:c.4977T=
MANE Select
|
NP_203699.1:p.Asp1659=
|
|