ENST00000367698.4:c.995C>T
MANE Select
|
ENSP00000356671.3:p.Thr332Ile
|
|
ENST00000367698.3:c.995C>T
|
ENSP00000356671.3:p.Thr332Ile
|
|
ENST00000617423.4:c.559+2154C>T
|
ENSP00000478688.1:n.559+2154C>T
|
|
NM_000488.3:c.995C>T , LRG_577t1:c.995C>T
|
NP_000479.1:p.Thr332Ile
|
|
XM_005245198.2:c.851C>T
|
XP_005245255.1:p.Thr284Ile
|
|
NM_001365052.1:c.851C>T
|
NP_001351981.1:p.Thr284Ile
|
|
NM_000488.4:c.995C>T
MANE Select
|
NP_000479.1:p.Thr332Ile
|
|
NM_001365052.2:c.851C>T
|
NP_001351981.1:p.Thr284Ile
|
|
NM_001386302.1:c.1118C>T
|
NP_001373231.1:p.Thr373Ile
|
|
NM_001386303.1:c.1076C>T
|
NP_001373232.1:p.Thr359Ile
|
|
NM_001386304.1:c.974C>T
|
NP_001373233.1:p.Thr325Ile
|
|
NM_001386305.1:c.938C>T
|
NP_001373234.1:p.Thr313Ile
|
|
NM_001386306.1:c.779C>T
|
NP_001373235.1:p.Thr260Ile
|
|