ENST00000328300.11:c.4738A>T
MANE Select
|
ENSP00000331902.7:p.Ile1580Phe
|
|
ENST00000361603.7:c.4720A>T
|
ENSP00000354505.2:p.Ile1574Phe
|
|
ENST00000510690.2:n.1232A>T
|
|
|
ENST00000644079.1:n.1224A>T
|
|
|
ENST00000328300.10:c.4738A>T
|
ENSP00000331902.6:p.Ile1580Phe
|
|
ENST00000361603.6:c.4720A>T
|
ENSP00000354505.2:p.Ile1574Phe
|
|
ENST00000504541.1:c.136A>T
|
ENSP00000424845.1:p.Ile46Phe
|
|
ENST00000515658.1:c.325-1459A>T
|
|
|
NM_000495.4:c.4720A>T
|
NP_000486.1:p.Ile1574Phe
|
|
NM_033380.2:c.4738A>T
|
NP_203699.1:p.Ile1580Phe
|
|
XM_005262070.2:c.4729A>T
|
XP_005262127.1:p.Ile1577Phe
|
|
XM_006724616.2:c.4738A>T
|
XP_006724679.1:p.Ile1580Phe
|
|
XM_011530849.1:c.4414A>T
|
XP_011529151.1:p.Ile1472Phe
|
|
XM_011530851.1:c.2311A>T
|
XP_011529153.1:p.Ile771Phe
|
|
XM_011530849.2:c.4753A>T
|
XP_011529151.2:p.Ile1585Phe
|
|
XM_017029259.2:c.4744A>T
|
XP_016884748.1:p.Ile1582Phe
|
|
XM_017029260.1:c.4735A>T
|
XP_016884749.1:p.Ile1579Phe
|
|
XM_017029263.2:c.3073A>T
|
XP_016884752.1:p.Ile1025Phe
|
|
NM_000495.5:c.4720A>T
|
NP_000486.1:p.Ile1574Phe
|
|
NM_033380.3:c.4738A>T
MANE Select
|
NP_203699.1:p.Ile1580Phe
|
|