ENST00000588328.7:c.932G>T
|
ENSP00000468516.4:p.Arg311Leu
|
|
ENST00000651901.2:c.932G>T
|
ENSP00000498922.2:p.Arg311Leu
|
|
ENST00000698359.1:c.887G>T
|
ENSP00000513682.1:p.Arg296Leu
|
|
ENST00000698360.1:c.983G>T
|
ENSP00000513683.1:p.Arg328Leu
|
|
ENST00000698361.1:c.932G>T
|
ENSP00000513684.1:p.Arg311Leu
|
|
ENST00000698362.1:c.932G>T
|
ENSP00000513685.1:p.Arg311Leu
|
|
ENST00000698363.1:n.995G>T
|
|
|
ENST00000698364.1:n.995G>T
|
|
|
ENST00000698365.1:n.995G>T
|
|
|
ENST00000698426.1:c.611G>T
|
ENSP00000513713.1:p.Arg204Leu
|
|
ENST00000698427.1:c.974G>T
|
ENSP00000513714.1:p.Arg325Leu
|
|
ENST00000698428.1:c.611G>T
|
ENSP00000513715.1:p.Arg204Leu
|
|
ENST00000698429.1:n.815G>T
|
|
|
ENST00000698430.1:c.1182G>T
|
|
|
ENST00000698431.1:c.669G>T
|
ENSP00000513717.1:n.669G>T
|
|
ENST00000698432.1:c.741G>T
|
|
|
ENST00000698433.1:n.394G>T
|
|
|
ENST00000698434.1:n.419G>T
|
|
|
ENST00000244137.12:c.932G>T
MANE Select
|
ENSP00000244137.5:p.Arg311Leu
|
|
ENST00000588328.6:c.921G>T
|
|
|
ENST00000590731.6:n.607G>T
|
|
|
ENST00000651901.1:c.928G>T
|
|
|
ENST00000244137.11:c.932G>T
|
ENSP00000244137.5:p.Arg311Leu
|
|
ENST00000397032.8:c.809G>T
|
ENSP00000380226.3:p.Arg270Leu
|
|
ENST00000436370.7:c.740G>T
|
ENSP00000391890.2:p.Arg247Leu
|
|
ENST00000588328.5:c.423G>T
|
|
|
NM_000285.3:c.932G>T
|
NP_000276.2:p.Arg311Leu
|
|
NM_001166056.1:c.809G>T
|
NP_001159528.1:p.Arg270Leu
|
|
NM_001166057.1:c.740G>T
|
NP_001159529.1:p.Arg247Leu
|
|
NM_000285.4:c.932G>T
MANE Select
|
NP_000276.2:p.Arg311Leu
|
|
NM_001166056.2:c.809G>T
|
NP_001159528.1:p.Arg270Leu
|
|
NM_001166057.2:c.740G>T
|
NP_001159529.1:p.Arg247Leu
|
|