ENST00000367698.4:c.1331T>A
MANE Select
|
ENSP00000356671.3:p.Ile444Lys
|
|
ENST00000367698.3:c.1331T>A
|
ENSP00000356671.3:p.Ile444Lys
|
|
ENST00000617423.4:c.716T>A
|
ENSP00000478688.1:p.Ile239Lys
|
|
NM_000488.3:c.1331T>A , LRG_577t1:c.1331T>A
|
NP_000479.1:p.Ile444Lys
|
|
XM_005245198.2:c.1187T>A
|
XP_005245255.1:p.Ile396Lys
|
|
NM_001365052.1:c.1187T>A
|
NP_001351981.1:p.Ile396Lys
|
|
NM_000488.4:c.1331T>A
MANE Select
|
NP_000479.1:p.Ile444Lys
|
|
NM_001365052.2:c.1187T>A
|
NP_001351981.1:p.Ile396Lys
|
|
NM_001386302.1:c.1454T>A
|
NP_001373231.1:p.Ile485Lys
|
|
NM_001386303.1:c.1412T>A
|
NP_001373232.1:p.Ile471Lys
|
|
NM_001386304.1:c.1310T>A
|
NP_001373233.1:p.Ile437Lys
|
|
NM_001386305.1:c.1274T>A
|
NP_001373234.1:p.Ile425Lys
|
|
NM_001386306.1:c.1115T>A
|
NP_001373235.1:p.Ile372Lys
|
|