ENST00000328300.11:c.4127T>C
MANE Select
|
ENSP00000331902.7:p.Ile1376Thr
|
|
ENST00000361603.7:c.4109T>C
|
ENSP00000354505.2:p.Ile1370Thr
|
|
ENST00000510690.2:n.621T>C
|
|
|
ENST00000328300.10:c.4127T>C
|
ENSP00000331902.6:p.Ile1376Thr
|
|
ENST00000361603.6:c.4109T>C
|
ENSP00000354505.2:p.Ile1370Thr
|
|
ENST00000489230.1:n.530T>C
|
|
|
NM_000495.4:c.4109T>C
|
NP_000486.1:p.Ile1370Thr
|
|
NM_033380.2:c.4127T>C
|
NP_203699.1:p.Ile1376Thr
|
|
XM_005262070.2:c.4118T>C
|
XP_005262127.1:p.Ile1373Thr
|
|
XM_006724616.2:c.4127T>C
|
XP_006724679.1:p.Ile1376Thr
|
|
XM_011530849.1:c.3803T>C
|
XP_011529151.1:p.Ile1268Thr
|
|
XM_011530851.1:c.1700T>C
|
XP_011529153.1:p.Ile567Thr
|
|
XM_011530849.2:c.4142T>C
|
XP_011529151.2:p.Ile1381Thr
|
|
XM_017029259.2:c.4133T>C
|
XP_016884748.1:p.Ile1378Thr
|
|
XM_017029260.1:c.4124T>C
|
XP_016884749.1:p.Ile1375Thr
|
|
XM_017029263.2:c.2462T>C
|
XP_016884752.1:p.Ile821Thr
|
|
NM_000495.5:c.4109T>C
|
NP_000486.1:p.Ile1370Thr
|
|
NM_033380.3:c.4127T>C
MANE Select
|
NP_203699.1:p.Ile1376Thr
|
|