ENST00000328300.11:c.4295C>G
MANE Select
|
ENSP00000331902.7:p.Pro1432Arg
|
|
ENST00000361603.7:c.4277C>G
|
ENSP00000354505.2:p.Pro1426Arg
|
|
ENST00000510690.2:n.789C>G
|
|
|
ENST00000328300.10:c.4295C>G
|
ENSP00000331902.6:p.Pro1432Arg
|
|
ENST00000361603.6:c.4277C>G
|
ENSP00000354505.2:p.Pro1426Arg
|
|
ENST00000489230.1:n.698C>G
|
|
|
ENST00000515658.1:c.91C>G
|
|
|
NM_000495.4:c.4277C>G
|
NP_000486.1:p.Pro1426Arg
|
|
NM_033380.2:c.4295C>G
|
NP_203699.1:p.Pro1432Arg
|
|
XM_005262070.2:c.4286C>G
|
XP_005262127.1:p.Pro1429Arg
|
|
XM_006724616.2:c.4295C>G
|
XP_006724679.1:p.Pro1432Arg
|
|
XM_011530849.1:c.3971C>G
|
XP_011529151.1:p.Pro1324Arg
|
|
XM_011530851.1:c.1868C>G
|
XP_011529153.1:p.Pro623Arg
|
|
XM_011530849.2:c.4310C>G
|
XP_011529151.2:p.Pro1437Arg
|
|
XM_017029259.2:c.4301C>G
|
XP_016884748.1:p.Pro1434Arg
|
|
XM_017029260.1:c.4292C>G
|
XP_016884749.1:p.Pro1431Arg
|
|
XM_017029263.2:c.2630C>G
|
XP_016884752.1:p.Pro877Arg
|
|
NM_000495.5:c.4277C>G
|
NP_000486.1:p.Pro1426Arg
|
|
NM_033380.3:c.4295C>G
MANE Select
|
NP_203699.1:p.Pro1432Arg
|
|