ENST00000454220.7:c.669G>T
|
ENSP00000391905.3:p.Arg223=
|
|
ENST00000703395.1:c.12G>T
|
ENSP00000515286.1:p.Arg4=
|
|
ENST00000703396.1:n.493G>T
|
|
|
ENST00000703397.1:c.12G>T
|
ENSP00000515287.1:p.Arg4=
|
|
ENST00000703398.1:c.591G>T
|
ENSP00000515288.1:p.Arg197=
|
|
ENST00000703421.1:n.702G>T
|
|
|
ENST00000703422.1:c.525G>T
|
ENSP00000515292.1:p.Arg175=
|
|
ENST00000703423.1:c.12G>T
|
ENSP00000515293.1:p.Arg4=
|
|
ENST00000322088.11:c.549G>T
MANE Select
|
ENSP00000324804.6:p.Arg183=
|
|
ENST00000322088.10:c.549G>T
|
ENSP00000324804.6:p.Arg183=
|
|
ENST00000454220.6:c.669G>T
|
ENSP00000391905.2:p.Arg223=
|
|
ENST00000462047.1:n.240G>T
|
|
|
ENST00000462990.5:c.12G>T
|
ENSP00000470504.1:p.Arg4=
|
|
NM_014225.5:c.549G>T
|
NP_055040.2:p.Arg183=
|
|
NR_033500.1:n.743G>T
|
|
|
NM_001363656.1:c.12G>T
|
NP_001350585.1:p.Arg4=
|
|
NM_014225.6:c.549G>T
MANE Select
|
NP_055040.2:p.Arg183=
|
|
NM_001363656.2:c.12G>T
|
NP_001350585.1:p.Arg4=
|
|
NR_033500.2:n.493G>T
|
|
|