|
NM_021939.4:c.505C>G
MANE Select
|
NP_068758.3:p.Arg169Gly
|
|
ENST00000321562.9:c.505C>G
MANE Select
|
ENSP00000317232.4:p.Arg169Gly
|
|
NM_021939.3:c.505C>G , LRG_12t1:c.505C>G
|
NP_068758.3:p.Arg169Gly
|
|
ENST00000321562.8:c.505C>G
|
ENSP00000317232.4:p.Arg169Gly
|
|
ENST00000489591.5:c.359C>G
|
ENSP00000466352.1:p.Pro120Arg
|
|
ENST00000585664.5:c.325C>G
|
ENSP00000468703.1:p.Arg109Gly
|
|
ENST00000585922.5:c.505C>G
|
ENSP00000466097.1:p.Arg169Gly
|
|
ENST00000706683.1:c.505C>G
|
ENSP00000516497.1:p.Arg169Gly
|
|
XM_011525099.1:c.505C>G
|
XP_011523401.1:p.Arg169Gly
|
|
XM_011525099.3:c.505C>G
|
XP_011523401.1:p.Arg169Gly
|
|
XM_011525100.1:c.232C>G
|
XP_011523402.1:p.Arg78Gly
|
|
XM_011525100.2:c.232C>G
|
XP_011523402.1:p.Arg78Gly
|