ENST00000367698.4:c.1353T>A
MANE Select
|
ENSP00000356671.3:p.Thr451=
|
|
ENST00000367698.3:c.1353T>A
|
ENSP00000356671.3:p.Thr451=
|
|
ENST00000617423.4:c.738T>A
|
ENSP00000478688.1:p.Thr246=
|
|
NM_000488.3:c.1353T>A , LRG_577t1:c.1353T>A
|
NP_000479.1:p.Thr451=
|
|
XM_005245198.2:c.1209T>A
|
XP_005245255.1:p.Thr403=
|
|
NM_001365052.1:c.1209T>A
|
NP_001351981.1:p.Thr403=
|
|
NM_000488.4:c.1353T>A
MANE Select
|
NP_000479.1:p.Thr451=
|
|
NM_001365052.2:c.1209T>A
|
NP_001351981.1:p.Thr403=
|
|
NM_001386302.1:c.1476T>A
|
NP_001373231.1:p.Thr492=
|
|
NM_001386303.1:c.1434T>A
|
NP_001373232.1:p.Thr478=
|
|
NM_001386304.1:c.1332T>A
|
NP_001373233.1:p.Thr444=
|
|
NM_001386305.1:c.1296T>A
|
NP_001373234.1:p.Thr432=
|
|
NM_001386306.1:c.1137T>A
|
NP_001373235.1:p.Thr379=
|
|