ENST00000328300.11:c.4768C>G
MANE Select
|
ENSP00000331902.7:p.Pro1590Ala
|
|
ENST00000361603.7:c.4750C>G
|
ENSP00000354505.2:p.Pro1584Ala
|
|
ENST00000510690.2:n.1262C>G
|
|
|
ENST00000644079.1:n.1254C>G
|
|
|
ENST00000328300.10:c.4768C>G
|
ENSP00000331902.6:p.Pro1590Ala
|
|
ENST00000361603.6:c.4750C>G
|
ENSP00000354505.2:p.Pro1584Ala
|
|
ENST00000504541.1:c.166C>G
|
ENSP00000424845.1:p.Pro56Ala
|
|
ENST00000515658.1:c.325-1429C>G
|
|
|
NM_000495.4:c.4750C>G
|
NP_000486.1:p.Pro1584Ala
|
|
NM_033380.2:c.4768C>G
|
NP_203699.1:p.Pro1590Ala
|
|
XM_005262070.2:c.4759C>G
|
XP_005262127.1:p.Pro1587Ala
|
|
XM_006724616.2:c.4768C>G
|
XP_006724679.1:p.Pro1590Ala
|
|
XM_011530849.1:c.4444C>G
|
XP_011529151.1:p.Pro1482Ala
|
|
XM_011530851.1:c.2341C>G
|
XP_011529153.1:p.Pro781Ala
|
|
XM_011530849.2:c.4783C>G
|
XP_011529151.2:p.Pro1595Ala
|
|
XM_017029259.2:c.4774C>G
|
XP_016884748.1:p.Pro1592Ala
|
|
XM_017029260.1:c.4765C>G
|
XP_016884749.1:p.Pro1589Ala
|
|
XM_017029263.2:c.3103C>G
|
XP_016884752.1:p.Pro1035Ala
|
|
NM_000495.5:c.4750C>G
|
NP_000486.1:p.Pro1584Ala
|
|
NM_033380.3:c.4768C>G
MANE Select
|
NP_203699.1:p.Pro1590Ala
|
|