ENST00000328300.11:c.4282C>A
MANE Select
|
ENSP00000331902.7:p.Arg1428Ser
|
|
ENST00000361603.7:c.4264C>A
|
ENSP00000354505.2:p.Arg1422Ser
|
|
ENST00000510690.2:n.776C>A
|
|
|
ENST00000328300.10:c.4282C>A
|
ENSP00000331902.6:p.Arg1428Ser
|
|
ENST00000361603.6:c.4264C>A
|
ENSP00000354505.2:p.Arg1422Ser
|
|
ENST00000489230.1:n.685C>A
|
|
|
ENST00000515658.1:c.78C>A
|
|
|
NM_000495.4:c.4264C>A
|
NP_000486.1:p.Arg1422Ser
|
|
NM_033380.2:c.4282C>A
|
NP_203699.1:p.Arg1428Ser
|
|
XM_005262070.2:c.4273C>A
|
XP_005262127.1:p.Arg1425Ser
|
|
XM_006724616.2:c.4282C>A
|
XP_006724679.1:p.Arg1428Ser
|
|
XM_011530849.1:c.3958C>A
|
XP_011529151.1:p.Arg1320Ser
|
|
XM_011530851.1:c.1855C>A
|
XP_011529153.1:p.Arg619Ser
|
|
XM_011530849.2:c.4297C>A
|
XP_011529151.2:p.Arg1433Ser
|
|
XM_017029259.2:c.4288C>A
|
XP_016884748.1:p.Arg1430Ser
|
|
XM_017029260.1:c.4279C>A
|
XP_016884749.1:p.Arg1427Ser
|
|
XM_017029263.2:c.2617C>A
|
XP_016884752.1:p.Arg873Ser
|
|
NM_000495.5:c.4264C>A
|
NP_000486.1:p.Arg1422Ser
|
|
NM_033380.3:c.4282C>A
MANE Select
|
NP_203699.1:p.Arg1428Ser
|
|