ENST00000367698.4:c.939G>A
MANE Select
|
ENSP00000356671.3:p.Met313Ile
|
|
ENST00000367698.3:c.939G>A
|
ENSP00000356671.3:p.Met313Ile
|
|
ENST00000487183.1:n.590G>A
|
|
|
ENST00000617423.4:c.559+2098G>A
|
ENSP00000478688.1:n.559+2098G>A
|
|
NM_000488.3:c.939G>A , LRG_577t1:c.939G>A
|
NP_000479.1:p.Met313Ile
|
|
XM_005245198.2:c.795G>A
|
XP_005245255.1:p.Met265Ile
|
|
NM_001365052.1:c.795G>A
|
NP_001351981.1:p.Met265Ile
|
|
NM_000488.4:c.939G>A
MANE Select
|
NP_000479.1:p.Met313Ile
|
|
NM_001365052.2:c.795G>A
|
NP_001351981.1:p.Met265Ile
|
|
NM_001386302.1:c.1062G>A
|
NP_001373231.1:p.Met354Ile
|
|
NM_001386303.1:c.1020G>A
|
NP_001373232.1:p.Met340Ile
|
|
NM_001386304.1:c.918G>A
|
NP_001373233.1:p.Met306Ile
|
|
NM_001386305.1:c.882G>A
|
NP_001373234.1:p.Met294Ile
|
|
NM_001386306.1:c.723G>A
|
NP_001373235.1:p.Met241Ile
|
|