ENST00000328300.11:c.4541G>A
MANE Select
|
ENSP00000331902.7:p.Ser1514Asn
|
|
ENST00000361603.7:c.4523G>A
|
ENSP00000354505.2:p.Ser1508Asn
|
|
ENST00000510690.2:n.1035G>A
|
|
|
ENST00000328300.10:c.4541G>A
|
ENSP00000331902.6:p.Ser1514Asn
|
|
ENST00000361603.6:c.4523G>A
|
ENSP00000354505.2:p.Ser1508Asn
|
|
ENST00000515658.1:c.325-3537G>A
|
|
|
NM_000495.4:c.4523G>A
|
NP_000486.1:p.Ser1508Asn
|
|
NM_033380.2:c.4541G>A
|
NP_203699.1:p.Ser1514Asn
|
|
XM_005262070.2:c.4532G>A
|
XP_005262127.1:p.Ser1511Asn
|
|
XM_006724616.2:c.4541G>A
|
XP_006724679.1:p.Ser1514Asn
|
|
XM_011530849.1:c.4217G>A
|
XP_011529151.1:p.Ser1406Asn
|
|
XM_011530851.1:c.2114G>A
|
XP_011529153.1:p.Ser705Asn
|
|
XM_011530849.2:c.4556G>A
|
XP_011529151.2:p.Ser1519Asn
|
|
XM_017029259.2:c.4547G>A
|
XP_016884748.1:p.Ser1516Asn
|
|
XM_017029260.1:c.4538G>A
|
XP_016884749.1:p.Ser1513Asn
|
|
XM_017029263.2:c.2876G>A
|
XP_016884752.1:p.Ser959Asn
|
|
NM_000495.5:c.4523G>A
|
NP_000486.1:p.Ser1508Asn
|
|
NM_033380.3:c.4541G>A
MANE Select
|
NP_203699.1:p.Ser1514Asn
|
|