ENST00000367698.4:c.1256C>G
MANE Select
|
ENSP00000356671.3:p.Ala419Gly
|
|
ENST00000367698.3:c.1256C>G
|
ENSP00000356671.3:p.Ala419Gly
|
|
ENST00000617423.4:c.641C>G
|
ENSP00000478688.1:p.Ala214Gly
|
|
NM_000488.3:c.1256C>G , LRG_577t1:c.1256C>G
|
NP_000479.1:p.Ala419Gly
|
|
XM_005245198.2:c.1112C>G
|
XP_005245255.1:p.Ala371Gly
|
|
NM_001365052.1:c.1112C>G
|
NP_001351981.1:p.Ala371Gly
|
|
NM_000488.4:c.1256C>G
MANE Select
|
NP_000479.1:p.Ala419Gly
|
|
NM_001365052.2:c.1112C>G
|
NP_001351981.1:p.Ala371Gly
|
|
NM_001386302.1:c.1379C>G
|
NP_001373231.1:p.Ala460Gly
|
|
NM_001386303.1:c.1337C>G
|
NP_001373232.1:p.Ala446Gly
|
|
NM_001386304.1:c.1235C>G
|
NP_001373233.1:p.Ala412Gly
|
|
NM_001386305.1:c.1199C>G
|
NP_001373234.1:p.Ala400Gly
|
|
NM_001386306.1:c.1040C>G
|
NP_001373235.1:p.Ala347Gly
|
|