|
ENST00000265909.9:c.2677T>G
MANE Select
|
ENSP00000265909.4:p.Phe893Val
|
|
|
ENST00000265909.8:c.2677T>G
|
ENSP00000265909.4:p.Phe893Val
|
|
|
ENST00000426933.6:c.181T>G
|
ENSP00000413345.2:p.Phe61Val
|
|
|
ENST00000526579.5:n.178-992T>G
|
|
|
|
ENST00000527116.5:n.439T>G
|
|
|
|
ENST00000528555.5:c.817T>G
|
ENSP00000435122.1:p.Phe273Val
|
|
|
ENST00000530330.1:n.413T>G
|
|
|
|
ENST00000530356.5:c.817T>G
|
ENSP00000432307.1:p.Phe273Val
|
|
|
ENST00000533318.5:n.1037T>G
|
|
|
|
ENST00000534726.5:c.397T>G
|
ENSP00000433699.1:p.Phe133Val
|
|
|
NM_001301089.1:c.817T>G
|
NP_001288018.1:p.Phe273Val
|
|
|
NM_014758.2:c.2677T>G
|
NP_055573.2:p.Phe893Val
|
|
|
XM_005271546.3:c.2574-992T>G
|
XP_005271603.1:n.2574-992T>G
|
|
|
XM_011542819.1:c.2923T>G
|
XP_011541121.1:p.Phe975Val
|
|
|
XM_011542820.1:c.2911T>G
|
XP_011541122.1:p.Phe971Val
|
|
|
XM_011542821.1:c.2803T>G
|
XP_011541123.1:p.Phe935Val
|
|
|
XM_011542824.1:c.2041T>G
|
XP_011541126.1:p.Phe681Val
|
|
|
XM_011542825.1:c.1198T>G
|
XP_011541127.1:p.Phe400Val
|
|
|
XM_011542826.1:c.1063T>G
|
XP_011541128.1:p.Phe355Val
|
|
|
XM_011542827.1:c.943T>G
|
XP_011541129.1:p.Phe315Val
|
|
|
NM_001347918.1:c.2557T>G
|
NP_001334847.1:p.Phe853Val
|
|
|
NM_001347919.1:c.2574-992T>G
|
NP_001334848.1:n.2574-992T>G
|
|
|
NM_001347922.1:c.1006T>G
|
NP_001334851.1:p.Phe336Val
|
|
|
NM_001347923.1:c.952T>G
|
NP_001334852.1:p.Phe318Val
|
|
|
NM_001347924.1:c.697T>G
|
NP_001334853.1:p.Phe233Val
|
|
|
NM_001347925.1:c.643T>G
|
NP_001334854.1:p.Phe215Val
|
|
|
NM_001347926.1:c.714-992T>G
|
NP_001334855.1:n.714-992T>G
|
|
|
NM_001347927.1:c.397T>G
|
NP_001334856.1:p.Phe133Val
|
|
|
NR_144939.1:n.3310T>G
|
|
|
|
XM_011542820.2:c.2911T>G
|
XP_011541122.1:p.Phe971Val
|
|
|
XM_011542821.3:c.2803T>G
|
XP_011541123.1:p.Phe935Val
|
|
|
XM_011542824.2:c.2041T>G
|
XP_011541126.1:p.Phe681Val
|
|
|
XM_011542825.2:c.1198T>G
|
XP_011541127.1:p.Phe400Val
|
|
|
XM_011542826.2:c.1063T>G
|
XP_011541128.1:p.Phe355Val
|
|
|
XM_024448521.1:c.2923T>G
|
XP_024304289.1:p.Phe975Val
|
|
|
XR_001747870.1:n.3748T>G
|
|
|
|
XR_001747872.1:n.3094T>G
|
|
|
|
XR_001747873.1:n.3408T>G
|
|
|
|
NM_001301089.2:c.817T>G
|
NP_001288018.1:p.Phe273Val
|
|
|
NM_001347918.2:c.2557T>G
|
NP_001334847.2:p.Phe853Val
|
|
|
NM_001347919.2:c.2574-992T>G
|
NP_001334848.2:n.2574-992T>G
|
|
|
NM_001347920.2:c.*21073T>G
|
NP_001334849.2:n.*21073T>G
|
|
|
NM_001347922.2:c.1006T>G
|
NP_001334851.2:p.Phe336Val
|
|
|
NM_001347923.2:c.952T>G
|
NP_001334852.2:p.Phe318Val
|
|
|
NM_001347924.2:c.697T>G
|
NP_001334853.1:p.Phe233Val
|
|
|
NM_001347925.2:c.643T>G
|
NP_001334854.1:p.Phe215Val
|
|
|
NM_001347926.2:c.714-992T>G
|
NP_001334855.1:n.714-992T>G
|
|
|
NM_001347927.2:c.397T>G
|
NP_001334856.1:p.Phe133Val
|
|
|
NM_014758.3:c.2677T>G
MANE Select
|
NP_055573.3:p.Phe893Val
|
|
|
NR_144939.2:n.3302T>G
|
|
|
