ENST00000367698.4:c.1266T>G
MANE Select
|
ENSP00000356671.3:p.Ile422Met
|
|
ENST00000367698.3:c.1266T>G
|
ENSP00000356671.3:p.Ile422Met
|
|
ENST00000617423.4:c.651T>G
|
ENSP00000478688.1:p.Ile217Met
|
|
NM_000488.3:c.1266T>G , LRG_577t1:c.1266T>G
|
NP_000479.1:p.Ile422Met
|
|
XM_005245198.2:c.1122T>G
|
XP_005245255.1:p.Ile374Met
|
|
NM_001365052.1:c.1122T>G
|
NP_001351981.1:p.Ile374Met
|
|
NM_000488.4:c.1266T>G
MANE Select
|
NP_000479.1:p.Ile422Met
|
|
NM_001365052.2:c.1122T>G
|
NP_001351981.1:p.Ile374Met
|
|
NM_001386302.1:c.1389T>G
|
NP_001373231.1:p.Ile463Met
|
|
NM_001386303.1:c.1347T>G
|
NP_001373232.1:p.Ile449Met
|
|
NM_001386304.1:c.1245T>G
|
NP_001373233.1:p.Ile415Met
|
|
NM_001386305.1:c.1209T>G
|
NP_001373234.1:p.Ile403Met
|
|
NM_001386306.1:c.1050T>G
|
NP_001373235.1:p.Ile350Met
|
|