ENST00000328300.11:c.4932T>C
MANE Select
|
ENSP00000331902.7:p.Cys1644=
|
|
ENST00000361603.7:c.4914T>C
|
ENSP00000354505.2:p.Cys1638=
|
|
ENST00000510690.2:n.1426T>C
|
|
|
ENST00000644079.1:n.1763T>C
|
|
|
ENST00000328300.10:c.4932T>C
|
ENSP00000331902.6:p.Cys1644=
|
|
ENST00000361603.6:c.4914T>C
|
ENSP00000354505.2:p.Cys1638=
|
|
ENST00000504541.1:c.219+456T>C
|
ENSP00000424845.1:n.219+456T>C
|
|
ENST00000515658.1:c.325-920T>C
|
|
|
NM_000495.4:c.4914T>C
|
NP_000486.1:p.Cys1638=
|
|
NM_033380.2:c.4932T>C
|
NP_203699.1:p.Cys1644=
|
|
XM_005262070.2:c.4923T>C
|
XP_005262127.1:p.Cys1641=
|
|
XM_006724616.2:c.4932T>C
|
XP_006724679.1:p.Cys1644=
|
|
XM_011530849.1:c.4608T>C
|
XP_011529151.1:p.Cys1536=
|
|
XM_011530851.1:c.2505T>C
|
XP_011529153.1:p.Cys835=
|
|
XM_011530849.2:c.4947T>C
|
XP_011529151.2:p.Cys1649=
|
|
XM_017029259.2:c.4938T>C
|
XP_016884748.1:p.Cys1646=
|
|
XM_017029260.1:c.4929T>C
|
XP_016884749.1:p.Cys1643=
|
|
XM_017029263.2:c.3267T>C
|
XP_016884752.1:p.Cys1089=
|
|
NM_000495.5:c.4914T>C
|
NP_000486.1:p.Cys1638=
|
|
NM_033380.3:c.4932T>C
MANE Select
|
NP_203699.1:p.Cys1644=
|
|