ENST00000334785.12:c.1347A>G
MANE Select
|
ENSP00000333938.7:p.Lys449=
|
|
ENST00000330010.12:c.1155A>G
|
ENSP00000327363.8:p.Lys385=
|
|
ENST00000334785.11:c.1347A>G
|
ENSP00000333938.7:p.Lys449=
|
|
ENST00000342754.5:c.1046A>G
|
|
|
ENST00000440324.5:c.1305A>G
|
ENSP00000411902.1:p.Lys435=
|
|
ENST00000464998.1:n.807A>G
|
|
|
ENST00000480732.2:n.921A>G
|
|
|
NM_001172309.1:c.1155A>G
|
NP_001165780.1:p.Lys385=
|
|
NM_144573.3:c.1347A>G , LRG_442t1:c.1347A>G
|
NP_653174.3:p.Lys449=
|
|
XM_005271322.2:c.1347A>G
|
XP_005271379.1:p.Lys449=
|
|
XM_005271323.2:c.1305A>G
|
XP_005271380.1:p.Lys435=
|
|
XM_005271324.3:c.1155A>G
|
XP_005271381.1:p.Lys385=
|
|
XM_005271325.2:c.1251+2439A>G
|
XP_005271382.1:n.1251+2439A>G
|
|
XM_005271326.2:c.1113A>G
|
XP_005271383.1:p.Lys371=
|
|
XM_005271327.2:c.930A>G
|
XP_005271384.1:p.Lys310=
|
|
XM_005271322.4:c.1347A>G
|
XP_005271379.1:p.Lys449=
|
|
XM_005271323.4:c.1305A>G
|
XP_005271380.1:p.Lys435=
|
|
XM_005271324.5:c.1155A>G
|
XP_005271381.1:p.Lys385=
|
|
XM_005271325.4:c.1251+2439A>G
|
XP_005271382.1:n.1251+2439A>G
|
|
XM_005271326.4:c.1113A>G
|
XP_005271383.1:p.Lys371=
|
|
XM_005271327.4:c.930A>G
|
XP_005271384.1:p.Lys310=
|
|
NM_001172309.2:c.1155A>G
|
NP_001165780.1:p.Lys385=
|
|
NM_144573.4:c.1347A>G
MANE Select
|
NP_653174.3:p.Lys449=
|
|