ENST00000265909.9:c.2634G>C
MANE Select
|
ENSP00000265909.4:p.Leu878=
|
|
ENST00000265909.8:c.2634G>C
|
ENSP00000265909.4:p.Leu878=
|
|
ENST00000426933.6:c.138G>C
|
ENSP00000413345.2:p.Leu46=
|
|
ENST00000526579.5:n.178-1035G>C
|
|
|
ENST00000527116.5:n.396G>C
|
|
|
ENST00000528555.5:c.774G>C
|
ENSP00000435122.1:p.Leu258=
|
|
ENST00000530330.1:n.370G>C
|
|
|
ENST00000530356.5:c.774G>C
|
ENSP00000432307.1:p.Leu258=
|
|
ENST00000533318.5:n.994G>C
|
|
|
ENST00000534726.5:c.354G>C
|
ENSP00000433699.1:p.Leu118=
|
|
NM_001301089.1:c.774G>C
|
NP_001288018.1:p.Leu258=
|
|
NM_014758.2:c.2634G>C
|
NP_055573.2:p.Leu878=
|
|
XM_005271546.3:c.2574-1035G>C
|
XP_005271603.1:n.2574-1035G>C
|
|
XM_011542819.1:c.2880G>C
|
XP_011541121.1:p.Leu960=
|
|
XM_011542820.1:c.2868G>C
|
XP_011541122.1:p.Leu956=
|
|
XM_011542821.1:c.2760G>C
|
XP_011541123.1:p.Leu920=
|
|
XM_011542824.1:c.1998G>C
|
XP_011541126.1:p.Leu666=
|
|
XM_011542825.1:c.1155G>C
|
XP_011541127.1:p.Leu385=
|
|
XM_011542826.1:c.1020G>C
|
XP_011541128.1:p.Leu340=
|
|
XM_011542827.1:c.900G>C
|
XP_011541129.1:p.Leu300=
|
|
NM_001347918.1:c.2514G>C
|
NP_001334847.1:p.Leu838=
|
|
NM_001347919.1:c.2574-1035G>C
|
NP_001334848.1:n.2574-1035G>C
|
|
NM_001347922.1:c.963G>C
|
NP_001334851.1:p.Leu321=
|
|
NM_001347923.1:c.909G>C
|
NP_001334852.1:p.Leu303=
|
|
NM_001347924.1:c.654G>C
|
NP_001334853.1:p.Leu218=
|
|
NM_001347925.1:c.600G>C
|
NP_001334854.1:p.Leu200=
|
|
NM_001347926.1:c.714-1035G>C
|
NP_001334855.1:n.714-1035G>C
|
|
NM_001347927.1:c.354G>C
|
NP_001334856.1:p.Leu118=
|
|
NR_144939.1:n.3267G>C
|
|
|
XM_011542820.2:c.2868G>C
|
XP_011541122.1:p.Leu956=
|
|
XM_011542821.3:c.2760G>C
|
XP_011541123.1:p.Leu920=
|
|
XM_011542824.2:c.1998G>C
|
XP_011541126.1:p.Leu666=
|
|
XM_011542825.2:c.1155G>C
|
XP_011541127.1:p.Leu385=
|
|
XM_011542826.2:c.1020G>C
|
XP_011541128.1:p.Leu340=
|
|
XM_024448521.1:c.2880G>C
|
XP_024304289.1:p.Leu960=
|
|
XR_001747870.1:n.3705G>C
|
|
|
XR_001747872.1:n.3051G>C
|
|
|
XR_001747873.1:n.3365G>C
|
|
|
NM_001301089.2:c.774G>C
|
NP_001288018.1:p.Leu258=
|
|
NM_001347918.2:c.2514G>C
|
NP_001334847.2:p.Leu838=
|
|
NM_001347919.2:c.2574-1035G>C
|
NP_001334848.2:n.2574-1035G>C
|
|
NM_001347920.2:c.*21030G>C
|
NP_001334849.2:n.*21030G>C
|
|
NM_001347922.2:c.963G>C
|
NP_001334851.2:p.Leu321=
|
|
NM_001347923.2:c.909G>C
|
NP_001334852.2:p.Leu303=
|
|
NM_001347924.2:c.654G>C
|
NP_001334853.1:p.Leu218=
|
|
NM_001347925.2:c.600G>C
|
NP_001334854.1:p.Leu200=
|
|
NM_001347926.2:c.714-1035G>C
|
NP_001334855.1:n.714-1035G>C
|
|
NM_001347927.2:c.354G>C
|
NP_001334856.1:p.Leu118=
|
|
NM_014758.3:c.2634G>C
MANE Select
|
NP_055573.3:p.Leu878=
|
|
NR_144939.2:n.3259G>C
|
|
|