ENST00000411641.7:c.579C>G
MANE Select
|
ENSP00000393887.2:p.Leu193=
|
|
ENST00000273784.5:c.582C>G
|
ENSP00000273784.5:p.Leu194=
|
|
ENST00000411641.6:c.579C>G
|
ENSP00000393887.2:p.Leu193=
|
|
NM_001622.2:c.579C>G
|
NP_001613.2:p.Leu193=
|
|
NM_001354571.1:c.582C>G
|
NP_001341500.1:p.Leu194=
|
|
NM_001354572.1:c.576C>G
|
NP_001341501.1:p.Leu192=
|
|
NM_001354573.1:c.579C>G
|
NP_001341502.1:p.Leu193=
|
|
NM_001622.3:c.579C>G
|
NP_001613.2:p.Leu193=
|
|
NM_001622.4:c.579C>G
MANE Select
|
NP_001613.2:p.Leu193=
|
|
NM_001354571.2:c.582C>G
|
NP_001341500.1:p.Leu194=
|
|
NM_001354572.2:c.576C>G
|
NP_001341501.1:p.Leu192=
|
|
NM_001354573.2:c.579C>G
|
NP_001341502.1:p.Leu193=
|
|