ENST00000454220.7:c.755T>G
|
ENSP00000391905.3:p.Leu252Arg
|
|
ENST00000703395.1:c.98T>G
|
ENSP00000515286.1:p.Leu33Arg
|
|
ENST00000703396.1:n.579T>G
|
|
|
ENST00000703397.1:c.98T>G
|
ENSP00000515287.1:p.Leu33Arg
|
|
ENST00000703398.1:c.677T>G
|
ENSP00000515288.1:p.Leu226Arg
|
|
ENST00000703421.1:n.788T>G
|
|
|
ENST00000703422.1:c.611T>G
|
ENSP00000515292.1:p.Leu204Arg
|
|
ENST00000703423.1:c.98T>G
|
ENSP00000515293.1:p.Leu33Arg
|
|
ENST00000322088.11:c.635T>G
MANE Select
|
ENSP00000324804.6:p.Leu212Arg
|
|
ENST00000322088.10:c.635T>G
|
ENSP00000324804.6:p.Leu212Arg
|
|
ENST00000454220.6:c.755T>G
|
ENSP00000391905.2:p.Leu252Arg
|
|
ENST00000462047.1:n.326T>G
|
|
|
ENST00000462990.5:c.98T>G
|
ENSP00000470504.1:p.Leu33Arg
|
|
NM_014225.5:c.635T>G
|
NP_055040.2:p.Leu212Arg
|
|
NR_033500.1:n.829T>G
|
|
|
NM_001363656.1:c.98T>G
|
NP_001350585.1:p.Leu33Arg
|
|
NM_014225.6:c.635T>G
MANE Select
|
NP_055040.2:p.Leu212Arg
|
|
NM_001363656.2:c.98T>G
|
NP_001350585.1:p.Leu33Arg
|
|
NR_033500.2:n.579T>G
|
|
|