ENST00000328300.11:c.4984G>C
MANE Select
|
ENSP00000331902.7:p.Asp1662His
|
|
ENST00000361603.7:c.4966G>C
|
ENSP00000354505.2:p.Asp1656His
|
|
ENST00000510690.2:n.1478G>C
|
|
|
ENST00000644079.1:n.1815G>C
|
|
|
ENST00000328300.10:c.4984G>C
|
ENSP00000331902.6:p.Asp1662His
|
|
ENST00000361603.6:c.4966G>C
|
ENSP00000354505.2:p.Asp1656His
|
|
ENST00000504541.1:c.219+508G>C
|
ENSP00000424845.1:n.219+508G>C
|
|
ENST00000515658.1:c.325-868G>C
|
|
|
NM_000495.4:c.4966G>C
|
NP_000486.1:p.Asp1656His
|
|
NM_033380.2:c.4984G>C
|
NP_203699.1:p.Asp1662His
|
|
XM_005262070.2:c.4975G>C
|
XP_005262127.1:p.Asp1659His
|
|
XM_006724616.2:c.4984G>C
|
XP_006724679.1:p.Asp1662His
|
|
XM_011530849.1:c.4660G>C
|
XP_011529151.1:p.Asp1554His
|
|
XM_011530851.1:c.2557G>C
|
XP_011529153.1:p.Asp853His
|
|
XM_011530849.2:c.4999G>C
|
XP_011529151.2:p.Asp1667His
|
|
XM_017029259.2:c.4990G>C
|
XP_016884748.1:p.Asp1664His
|
|
XM_017029260.1:c.4981G>C
|
XP_016884749.1:p.Asp1661His
|
|
XM_017029263.2:c.3319G>C
|
XP_016884752.1:p.Asp1107His
|
|
NM_000495.5:c.4966G>C
|
NP_000486.1:p.Asp1656His
|
|
NM_033380.3:c.4984G>C
MANE Select
|
NP_203699.1:p.Asp1662His
|
|