ENST00000367698.4:c.1268C>G
MANE Select
|
ENSP00000356671.3:p.Ala423Gly
|
|
ENST00000367698.3:c.1268C>G
|
ENSP00000356671.3:p.Ala423Gly
|
|
ENST00000617423.4:c.653C>G
|
ENSP00000478688.1:p.Ala218Gly
|
|
NM_000488.3:c.1268C>G , LRG_577t1:c.1268C>G
|
NP_000479.1:p.Ala423Gly
|
|
XM_005245198.2:c.1124C>G
|
XP_005245255.1:p.Ala375Gly
|
|
NM_001365052.1:c.1124C>G
|
NP_001351981.1:p.Ala375Gly
|
|
NM_000488.4:c.1268C>G
MANE Select
|
NP_000479.1:p.Ala423Gly
|
|
NM_001365052.2:c.1124C>G
|
NP_001351981.1:p.Ala375Gly
|
|
NM_001386302.1:c.1391C>G
|
NP_001373231.1:p.Ala464Gly
|
|
NM_001386303.1:c.1349C>G
|
NP_001373232.1:p.Ala450Gly
|
|
NM_001386304.1:c.1247C>G
|
NP_001373233.1:p.Ala416Gly
|
|
NM_001386305.1:c.1211C>G
|
NP_001373234.1:p.Ala404Gly
|
|
NM_001386306.1:c.1052C>G
|
NP_001373235.1:p.Ala351Gly
|
|