ENST00000265909.9:c.2640T>A
MANE Select
|
ENSP00000265909.4:p.Leu880=
|
|
ENST00000265909.8:c.2640T>A
|
ENSP00000265909.4:p.Leu880=
|
|
ENST00000426933.6:c.144T>A
|
ENSP00000413345.2:p.Leu48=
|
|
ENST00000526579.5:n.178-1029T>A
|
|
|
ENST00000527116.5:n.402T>A
|
|
|
ENST00000528555.5:c.780T>A
|
ENSP00000435122.1:p.Leu260=
|
|
ENST00000530330.1:n.376T>A
|
|
|
ENST00000530356.5:c.780T>A
|
ENSP00000432307.1:p.Leu260=
|
|
ENST00000533318.5:n.1000T>A
|
|
|
ENST00000534726.5:c.360T>A
|
ENSP00000433699.1:p.Leu120=
|
|
NM_001301089.1:c.780T>A
|
NP_001288018.1:p.Leu260=
|
|
NM_014758.2:c.2640T>A
|
NP_055573.2:p.Leu880=
|
|
XM_005271546.3:c.2574-1029T>A
|
XP_005271603.1:n.2574-1029T>A
|
|
XM_011542819.1:c.2886T>A
|
XP_011541121.1:p.Leu962=
|
|
XM_011542820.1:c.2874T>A
|
XP_011541122.1:p.Leu958=
|
|
XM_011542821.1:c.2766T>A
|
XP_011541123.1:p.Leu922=
|
|
XM_011542824.1:c.2004T>A
|
XP_011541126.1:p.Leu668=
|
|
XM_011542825.1:c.1161T>A
|
XP_011541127.1:p.Leu387=
|
|
XM_011542826.1:c.1026T>A
|
XP_011541128.1:p.Leu342=
|
|
XM_011542827.1:c.906T>A
|
XP_011541129.1:p.Leu302=
|
|
NM_001347918.1:c.2520T>A
|
NP_001334847.1:p.Leu840=
|
|
NM_001347919.1:c.2574-1029T>A
|
NP_001334848.1:n.2574-1029T>A
|
|
NM_001347922.1:c.969T>A
|
NP_001334851.1:p.Leu323=
|
|
NM_001347923.1:c.915T>A
|
NP_001334852.1:p.Leu305=
|
|
NM_001347924.1:c.660T>A
|
NP_001334853.1:p.Leu220=
|
|
NM_001347925.1:c.606T>A
|
NP_001334854.1:p.Leu202=
|
|
NM_001347926.1:c.714-1029T>A
|
NP_001334855.1:n.714-1029T>A
|
|
NM_001347927.1:c.360T>A
|
NP_001334856.1:p.Leu120=
|
|
NR_144939.1:n.3273T>A
|
|
|
XM_011542820.2:c.2874T>A
|
XP_011541122.1:p.Leu958=
|
|
XM_011542821.3:c.2766T>A
|
XP_011541123.1:p.Leu922=
|
|
XM_011542824.2:c.2004T>A
|
XP_011541126.1:p.Leu668=
|
|
XM_011542825.2:c.1161T>A
|
XP_011541127.1:p.Leu387=
|
|
XM_011542826.2:c.1026T>A
|
XP_011541128.1:p.Leu342=
|
|
XM_024448521.1:c.2886T>A
|
XP_024304289.1:p.Leu962=
|
|
XR_001747870.1:n.3711T>A
|
|
|
XR_001747872.1:n.3057T>A
|
|
|
XR_001747873.1:n.3371T>A
|
|
|
NM_001301089.2:c.780T>A
|
NP_001288018.1:p.Leu260=
|
|
NM_001347918.2:c.2520T>A
|
NP_001334847.2:p.Leu840=
|
|
NM_001347919.2:c.2574-1029T>A
|
NP_001334848.2:n.2574-1029T>A
|
|
NM_001347920.2:c.*21036T>A
|
NP_001334849.2:n.*21036T>A
|
|
NM_001347922.2:c.969T>A
|
NP_001334851.2:p.Leu323=
|
|
NM_001347923.2:c.915T>A
|
NP_001334852.2:p.Leu305=
|
|
NM_001347924.2:c.660T>A
|
NP_001334853.1:p.Leu220=
|
|
NM_001347925.2:c.606T>A
|
NP_001334854.1:p.Leu202=
|
|
NM_001347926.2:c.714-1029T>A
|
NP_001334855.1:n.714-1029T>A
|
|
NM_001347927.2:c.360T>A
|
NP_001334856.1:p.Leu120=
|
|
NM_014758.3:c.2640T>A
MANE Select
|
NP_055573.3:p.Leu880=
|
|
NR_144939.2:n.3265T>A
|
|
|