ENST00000367698.4:c.1264A>G
MANE Select
|
ENSP00000356671.3:p.Ile422Val
|
|
ENST00000367698.3:c.1264A>G
|
ENSP00000356671.3:p.Ile422Val
|
|
ENST00000617423.4:c.649A>G
|
ENSP00000478688.1:p.Ile217Val
|
|
NM_000488.3:c.1264A>G , LRG_577t1:c.1264A>G
|
NP_000479.1:p.Ile422Val
|
|
XM_005245198.2:c.1120A>G
|
XP_005245255.1:p.Ile374Val
|
|
NM_001365052.1:c.1120A>G
|
NP_001351981.1:p.Ile374Val
|
|
NM_000488.4:c.1264A>G
MANE Select
|
NP_000479.1:p.Ile422Val
|
|
NM_001365052.2:c.1120A>G
|
NP_001351981.1:p.Ile374Val
|
|
NM_001386302.1:c.1387A>G
|
NP_001373231.1:p.Ile463Val
|
|
NM_001386303.1:c.1345A>G
|
NP_001373232.1:p.Ile449Val
|
|
NM_001386304.1:c.1243A>G
|
NP_001373233.1:p.Ile415Val
|
|
NM_001386305.1:c.1207A>G
|
NP_001373234.1:p.Ile403Val
|
|
NM_001386306.1:c.1048A>G
|
NP_001373235.1:p.Ile350Val
|
|