ENST00000367698.4:c.1298C>T
MANE Select
|
ENSP00000356671.3:p.Thr433Ile
|
|
ENST00000367698.3:c.1298C>T
|
ENSP00000356671.3:p.Thr433Ile
|
|
ENST00000617423.4:c.683C>T
|
ENSP00000478688.1:p.Thr228Ile
|
|
NM_000488.3:c.1298C>T , LRG_577t1:c.1298C>T
|
NP_000479.1:p.Thr433Ile
|
|
XM_005245198.2:c.1154C>T
|
XP_005245255.1:p.Thr385Ile
|
|
NM_001365052.1:c.1154C>T
|
NP_001351981.1:p.Thr385Ile
|
|
NM_000488.4:c.1298C>T
MANE Select
|
NP_000479.1:p.Thr433Ile
|
|
NM_001365052.2:c.1154C>T
|
NP_001351981.1:p.Thr385Ile
|
|
NM_001386302.1:c.1421C>T
|
NP_001373231.1:p.Thr474Ile
|
|
NM_001386303.1:c.1379C>T
|
NP_001373232.1:p.Thr460Ile
|
|
NM_001386304.1:c.1277C>T
|
NP_001373233.1:p.Thr426Ile
|
|
NM_001386305.1:c.1241C>T
|
NP_001373234.1:p.Thr414Ile
|
|
NM_001386306.1:c.1082C>T
|
NP_001373235.1:p.Thr361Ile
|
|