ENST00000328300.11:c.4935C>T
MANE Select
|
ENSP00000331902.7:p.Asn1645=
|
|
ENST00000361603.7:c.4917C>T
|
ENSP00000354505.2:p.Asn1639=
|
|
ENST00000510690.2:n.1429C>T
|
|
|
ENST00000644079.1:n.1766C>T
|
|
|
ENST00000328300.10:c.4935C>T
|
ENSP00000331902.6:p.Asn1645=
|
|
ENST00000361603.6:c.4917C>T
|
ENSP00000354505.2:p.Asn1639=
|
|
ENST00000504541.1:c.219+459C>T
|
ENSP00000424845.1:n.219+459C>T
|
|
ENST00000515658.1:c.325-917C>T
|
|
|
NM_000495.4:c.4917C>T
|
NP_000486.1:p.Asn1639=
|
|
NM_033380.2:c.4935C>T
|
NP_203699.1:p.Asn1645=
|
|
XM_005262070.2:c.4926C>T
|
XP_005262127.1:p.Asn1642=
|
|
XM_006724616.2:c.4935C>T
|
XP_006724679.1:p.Asn1645=
|
|
XM_011530849.1:c.4611C>T
|
XP_011529151.1:p.Asn1537=
|
|
XM_011530851.1:c.2508C>T
|
XP_011529153.1:p.Asn836=
|
|
XM_011530849.2:c.4950C>T
|
XP_011529151.2:p.Asn1650=
|
|
XM_017029259.2:c.4941C>T
|
XP_016884748.1:p.Asn1647=
|
|
XM_017029260.1:c.4932C>T
|
XP_016884749.1:p.Asn1644=
|
|
XM_017029263.2:c.3270C>T
|
XP_016884752.1:p.Asn1090=
|
|
NM_000495.5:c.4917C>T
|
NP_000486.1:p.Asn1639=
|
|
NM_033380.3:c.4935C>T
MANE Select
|
NP_203699.1:p.Asn1645=
|
|