ENST00000328300.11:c.5015T>G
MANE Select
|
ENSP00000331902.7:p.Leu1672Arg
|
|
ENST00000361603.7:c.4997T>G
|
ENSP00000354505.2:p.Leu1666Arg
|
|
ENST00000510690.2:n.1509T>G
|
|
|
ENST00000644079.1:n.2703T>G
|
|
|
ENST00000328300.10:c.5015T>G
|
ENSP00000331902.6:p.Leu1672Arg
|
|
ENST00000361603.6:c.4997T>G
|
ENSP00000354505.2:p.Leu1666Arg
|
|
ENST00000504541.1:c.240T>G
|
ENSP00000424845.1:n.240T>G
|
|
ENST00000515658.1:c.345T>G
|
|
|
NM_000495.4:c.4997T>G
|
NP_000486.1:p.Leu1666Arg
|
|
NM_033380.2:c.5015T>G
|
NP_203699.1:p.Leu1672Arg
|
|
XM_005262070.2:c.5006T>G
|
XP_005262127.1:p.Leu1669Arg
|
|
XM_006724616.2:c.5015T>G
|
XP_006724679.1:p.Leu1672Arg
|
|
XM_011530849.1:c.4691T>G
|
XP_011529151.1:p.Leu1564Arg
|
|
XM_011530851.1:c.2588T>G
|
XP_011529153.1:p.Leu863Arg
|
|
XM_011530849.2:c.5030T>G
|
XP_011529151.2:p.Leu1677Arg
|
|
XM_017029259.2:c.5021T>G
|
XP_016884748.1:p.Leu1674Arg
|
|
XM_017029260.1:c.5012T>G
|
XP_016884749.1:p.Leu1671Arg
|
|
XM_017029263.2:c.3350T>G
|
XP_016884752.1:p.Leu1117Arg
|
|
NM_000495.5:c.4997T>G
|
NP_000486.1:p.Leu1666Arg
|
|
NM_033380.3:c.5015T>G
MANE Select
|
NP_203699.1:p.Leu1672Arg
|
|