ENST00000328300.11:c.4760T>A
MANE Select
|
ENSP00000331902.7:p.Ile1587Asn
|
|
ENST00000361603.7:c.4742T>A
|
ENSP00000354505.2:p.Ile1581Asn
|
|
ENST00000510690.2:n.1254T>A
|
|
|
ENST00000644079.1:n.1246T>A
|
|
|
ENST00000328300.10:c.4760T>A
|
ENSP00000331902.6:p.Ile1587Asn
|
|
ENST00000361603.6:c.4742T>A
|
ENSP00000354505.2:p.Ile1581Asn
|
|
ENST00000504541.1:c.158T>A
|
ENSP00000424845.1:p.Ile53Asn
|
|
ENST00000515658.1:c.325-1437T>A
|
|
|
NM_000495.4:c.4742T>A
|
NP_000486.1:p.Ile1581Asn
|
|
NM_033380.2:c.4760T>A
|
NP_203699.1:p.Ile1587Asn
|
|
XM_005262070.2:c.4751T>A
|
XP_005262127.1:p.Ile1584Asn
|
|
XM_006724616.2:c.4760T>A
|
XP_006724679.1:p.Ile1587Asn
|
|
XM_011530849.1:c.4436T>A
|
XP_011529151.1:p.Ile1479Asn
|
|
XM_011530851.1:c.2333T>A
|
XP_011529153.1:p.Ile778Asn
|
|
XM_011530849.2:c.4775T>A
|
XP_011529151.2:p.Ile1592Asn
|
|
XM_017029259.2:c.4766T>A
|
XP_016884748.1:p.Ile1589Asn
|
|
XM_017029260.1:c.4757T>A
|
XP_016884749.1:p.Ile1586Asn
|
|
XM_017029263.2:c.3095T>A
|
XP_016884752.1:p.Ile1032Asn
|
|
NM_000495.5:c.4742T>A
|
NP_000486.1:p.Ile1581Asn
|
|
NM_033380.3:c.4760T>A
MANE Select
|
NP_203699.1:p.Ile1587Asn
|
|