ENST00000328300.11:c.4312C>T
MANE Select
|
ENSP00000331902.7:p.Pro1438Ser
|
|
ENST00000361603.7:c.4294C>T
|
ENSP00000354505.2:p.Pro1432Ser
|
|
ENST00000510690.2:n.806C>T
|
|
|
ENST00000328300.10:c.4312C>T
|
ENSP00000331902.6:p.Pro1438Ser
|
|
ENST00000361603.6:c.4294C>T
|
ENSP00000354505.2:p.Pro1432Ser
|
|
ENST00000489230.1:n.715C>T
|
|
|
ENST00000515658.1:c.108C>T
|
|
|
NM_000495.4:c.4294C>T
|
NP_000486.1:p.Pro1432Ser
|
|
NM_033380.2:c.4312C>T
|
NP_203699.1:p.Pro1438Ser
|
|
XM_005262070.2:c.4303C>T
|
XP_005262127.1:p.Pro1435Ser
|
|
XM_006724616.2:c.4312C>T
|
XP_006724679.1:p.Pro1438Ser
|
|
XM_011530849.1:c.3988C>T
|
XP_011529151.1:p.Pro1330Ser
|
|
XM_011530851.1:c.1885C>T
|
XP_011529153.1:p.Pro629Ser
|
|
XM_011530849.2:c.4327C>T
|
XP_011529151.2:p.Pro1443Ser
|
|
XM_017029259.2:c.4318C>T
|
XP_016884748.1:p.Pro1440Ser
|
|
XM_017029260.1:c.4309C>T
|
XP_016884749.1:p.Pro1437Ser
|
|
XM_017029263.2:c.2647C>T
|
XP_016884752.1:p.Pro883Ser
|
|
NM_000495.5:c.4294C>T
|
NP_000486.1:p.Pro1432Ser
|
|
NM_033380.3:c.4312C>T
MANE Select
|
NP_203699.1:p.Pro1438Ser
|
|