ENST00000306010.8:c.534A>G
|
ENSP00000302111.7:p.Arg178=
|
|
ENST00000651593.1:c.441A>G
MANE Select
|
ENSP00000498729.1:p.Arg147=
|
|
ENST00000306010.7:c.534A>G
|
ENSP00000302111.7:p.Arg178=
|
|
NM_002412.3:c.534A>G
|
NP_002403.2:p.Arg178=
|
|
NM_002412.4:c.534A>G
|
NP_002403.2:p.Arg178=
|
|
XM_005252682.2:c.441A>G
|
XP_005252739.1:p.Arg147=
|
|
XM_006717863.2:c.264A>G
|
XP_006717926.1:p.Arg88=
|
|
XM_011539817.1:c.450A>G
|
XP_011538119.1:p.Arg150=
|
|
NM_002412.5:c.441A>G
MANE Select
|
NP_002403.3:p.Arg147=
|
|
XM_017016275.1:c.264A>G
|
XP_016871764.1:p.Arg88=
|
|