ENST00000328300.11:c.4994+405A>G
MANE Select
|
ENSP00000331902.7:n.4994+405A>G
|
|
ENST00000361603.7:c.4976+405A>G
|
ENSP00000354505.2:n.4976+405A>G
|
|
ENST00000510690.2:n.1488+405A>G
|
|
|
ENST00000644079.1:n.2230A>G
|
|
|
ENST00000328300.10:c.4994+405A>G
|
ENSP00000331902.6:n.4994+405A>G
|
|
ENST00000361603.6:c.4976+405A>G
|
ENSP00000354505.2:n.4976+405A>G
|
|
ENST00000504541.1:c.220-453A>G
|
ENSP00000424845.1:n.220-453A>G
|
|
ENST00000515658.1:c.325-453A>G
|
|
|
NM_000495.4:c.4976+405A>G
|
NP_000486.1:n.4976+405A>G
|
|
NM_033380.2:c.4994+405A>G
|
NP_203699.1:n.4994+405A>G
|
|
XM_005262070.2:c.4985+405A>G
|
XP_005262127.1:n.4985+405A>G
|
|
XM_006724616.2:c.4994+405A>G
|
XP_006724679.1:n.4994+405A>G
|
|
XM_011530849.1:c.4670+405A>G
|
XP_011529151.1:n.4670+405A>G
|
|
XM_011530851.1:c.2567+405A>G
|
XP_011529153.1:n.2567+405A>G
|
|
XM_011530849.2:c.5009+405A>G
|
XP_011529151.2:n.5009+405A>G
|
|
XM_017029259.2:c.5000+405A>G
|
XP_016884748.1:n.5000+405A>G
|
|
XM_017029260.1:c.4991+405A>G
|
XP_016884749.1:n.4991+405A>G
|
|
XM_017029263.2:c.3329+405A>G
|
XP_016884752.1:n.3329+405A>G
|
|
NM_000495.5:c.4976+405A>G
|
NP_000486.1:n.4976+405A>G
|
|
NM_033380.3:c.4994+405A>G
MANE Select
|
NP_203699.1:n.4994+405A>G
|
|