ENST00000328300.11:c.4947C>T
MANE Select
|
ENSP00000331902.7:p.Asn1649=
|
|
ENST00000361603.7:c.4929C>T
|
ENSP00000354505.2:p.Asn1643=
|
|
ENST00000510690.2:n.1441C>T
|
|
|
ENST00000644079.1:n.1778C>T
|
|
|
ENST00000328300.10:c.4947C>T
|
ENSP00000331902.6:p.Asn1649=
|
|
ENST00000361603.6:c.4929C>T
|
ENSP00000354505.2:p.Asn1643=
|
|
ENST00000504541.1:c.219+471C>T
|
ENSP00000424845.1:n.219+471C>T
|
|
ENST00000515658.1:c.325-905C>T
|
|
|
NM_000495.4:c.4929C>T
|
NP_000486.1:p.Asn1643=
|
|
NM_033380.2:c.4947C>T
|
NP_203699.1:p.Asn1649=
|
|
XM_005262070.2:c.4938C>T
|
XP_005262127.1:p.Asn1646=
|
|
XM_006724616.2:c.4947C>T
|
XP_006724679.1:p.Asn1649=
|
|
XM_011530849.1:c.4623C>T
|
XP_011529151.1:p.Asn1541=
|
|
XM_011530851.1:c.2520C>T
|
XP_011529153.1:p.Asn840=
|
|
XM_011530849.2:c.4962C>T
|
XP_011529151.2:p.Asn1654=
|
|
XM_017029259.2:c.4953C>T
|
XP_016884748.1:p.Asn1651=
|
|
XM_017029260.1:c.4944C>T
|
XP_016884749.1:p.Asn1648=
|
|
XM_017029263.2:c.3282C>T
|
XP_016884752.1:p.Asn1094=
|
|
NM_000495.5:c.4929C>T
|
NP_000486.1:p.Asn1643=
|
|
NM_033380.3:c.4947C>T
MANE Select
|
NP_203699.1:p.Asn1649=
|
|