ENST00000328300.11:c.3891dup
MANE Select
|
ENSP00000331902.7:p.Leu1298AlafsTer19
|
|
ENST00000361603.7:c.3873dup
|
ENSP00000354505.2:p.Leu1292AlafsTer19
|
|
ENST00000510690.2:n.385dup
|
|
|
ENST00000328300.10:c.3891dup
|
ENSP00000331902.6:p.Leu1298AlafsTer19
|
|
ENST00000361603.6:c.3873dup
|
ENSP00000354505.2:p.Leu1292AlafsTer19
|
|
ENST00000489230.1:n.294dup
|
|
|
NM_000495.4:c.3873dup
|
NP_000486.1:p.Leu1292AlafsTer19
|
|
NM_033380.2:c.3891dup
|
NP_203699.1:p.Leu1298AlafsTer19
|
|
XM_005262070.2:c.3882dup
|
XP_005262127.1:p.Leu1295AlafsTer19
|
|
XM_006724616.2:c.3891dup
|
XP_006724679.1:p.Leu1298AlafsTer19
|
|
XM_011530849.1:c.3567dup
|
XP_011529151.1:p.Leu1190AlafsTer19
|
|
XM_011530851.1:c.1464dup
|
XP_011529153.1:p.Leu489AlafsTer19
|
|
XM_011530849.2:c.3906dup
|
XP_011529151.2:p.Leu1303AlafsTer19
|
|
XM_017029259.2:c.3897dup
|
XP_016884748.1:p.Leu1300AlafsTer19
|
|
XM_017029260.1:c.3888dup
|
XP_016884749.1:p.Leu1297AlafsTer19
|
|
XM_017029261.1:c.3906dup
|
XP_016884750.1:p.Leu1303AlafsTer20
|
|
XM_017029263.2:c.2226dup
|
XP_016884752.1:p.Leu743AlafsTer19
|
|
NM_000495.5:c.3873dup
|
NP_000486.1:p.Leu1292AlafsTer19
|
|
NM_033380.3:c.3891dup
MANE Select
|
NP_203699.1:p.Leu1298AlafsTer19
|
|