ENST00000328300.11:c.4506A>G
MANE Select
|
ENSP00000331902.7:p.Lys1502=
|
|
ENST00000361603.7:c.4488A>G
|
ENSP00000354505.2:p.Lys1496=
|
|
ENST00000510690.2:n.1000A>G
|
|
|
ENST00000328300.10:c.4506A>G
|
ENSP00000331902.6:p.Lys1502=
|
|
ENST00000361603.6:c.4488A>G
|
ENSP00000354505.2:p.Lys1496=
|
|
ENST00000515658.1:c.302A>G
|
|
|
NM_000495.4:c.4488A>G
|
NP_000486.1:p.Lys1496=
|
|
NM_033380.2:c.4506A>G
|
NP_203699.1:p.Lys1502=
|
|
XM_005262070.2:c.4497A>G
|
XP_005262127.1:p.Lys1499=
|
|
XM_006724616.2:c.4506A>G
|
XP_006724679.1:p.Lys1502=
|
|
XM_011530849.1:c.4182A>G
|
XP_011529151.1:p.Lys1394=
|
|
XM_011530851.1:c.2079A>G
|
XP_011529153.1:p.Lys693=
|
|
XM_011530849.2:c.4521A>G
|
XP_011529151.2:p.Lys1507=
|
|
XM_017029259.2:c.4512A>G
|
XP_016884748.1:p.Lys1504=
|
|
XM_017029260.1:c.4503A>G
|
XP_016884749.1:p.Lys1501=
|
|
XM_017029263.2:c.2841A>G
|
XP_016884752.1:p.Lys947=
|
|
NM_000495.5:c.4488A>G
|
NP_000486.1:p.Lys1496=
|
|
NM_033380.3:c.4506A>G
MANE Select
|
NP_203699.1:p.Lys1502=
|
|