ENST00000265909.9:c.2686C>T
MANE Select
|
ENSP00000265909.4:p.Pro896Ser
|
|
ENST00000265909.8:c.2686C>T
|
ENSP00000265909.4:p.Pro896Ser
|
|
ENST00000426933.6:c.190C>T
|
ENSP00000413345.2:p.Pro64Ser
|
|
ENST00000526579.5:n.178-983C>T
|
|
|
ENST00000527116.5:n.448C>T
|
|
|
ENST00000528555.5:c.826C>T
|
ENSP00000435122.1:p.Pro276Ser
|
|
ENST00000530330.1:n.422C>T
|
|
|
ENST00000530356.5:c.826C>T
|
ENSP00000432307.1:p.Pro276Ser
|
|
ENST00000533318.5:n.1046C>T
|
|
|
ENST00000534726.5:c.406C>T
|
ENSP00000433699.1:p.Pro136Ser
|
|
NM_001301089.1:c.826C>T
|
NP_001288018.1:p.Pro276Ser
|
|
NM_014758.2:c.2686C>T
|
NP_055573.2:p.Pro896Ser
|
|
XM_005271546.3:c.2574-983C>T
|
XP_005271603.1:n.2574-983C>T
|
|
XM_011542819.1:c.2932C>T
|
XP_011541121.1:p.Pro978Ser
|
|
XM_011542820.1:c.2920C>T
|
XP_011541122.1:p.Pro974Ser
|
|
XM_011542821.1:c.2812C>T
|
XP_011541123.1:p.Pro938Ser
|
|
XM_011542824.1:c.2050C>T
|
XP_011541126.1:p.Pro684Ser
|
|
XM_011542825.1:c.1207C>T
|
XP_011541127.1:p.Pro403Ser
|
|
XM_011542826.1:c.1072C>T
|
XP_011541128.1:p.Pro358Ser
|
|
XM_011542827.1:c.952C>T
|
XP_011541129.1:p.Pro318Ser
|
|
NM_001347918.1:c.2566C>T
|
NP_001334847.1:p.Pro856Ser
|
|
NM_001347919.1:c.2574-983C>T
|
NP_001334848.1:n.2574-983C>T
|
|
NM_001347922.1:c.1015C>T
|
NP_001334851.1:p.Pro339Ser
|
|
NM_001347923.1:c.961C>T
|
NP_001334852.1:p.Pro321Ser
|
|
NM_001347924.1:c.706C>T
|
NP_001334853.1:p.Pro236Ser
|
|
NM_001347925.1:c.652C>T
|
NP_001334854.1:p.Pro218Ser
|
|
NM_001347926.1:c.714-983C>T
|
NP_001334855.1:n.714-983C>T
|
|
NM_001347927.1:c.406C>T
|
NP_001334856.1:p.Pro136Ser
|
|
NR_144939.1:n.3319C>T
|
|
|
XM_011542820.2:c.2920C>T
|
XP_011541122.1:p.Pro974Ser
|
|
XM_011542821.3:c.2812C>T
|
XP_011541123.1:p.Pro938Ser
|
|
XM_011542824.2:c.2050C>T
|
XP_011541126.1:p.Pro684Ser
|
|
XM_011542825.2:c.1207C>T
|
XP_011541127.1:p.Pro403Ser
|
|
XM_011542826.2:c.1072C>T
|
XP_011541128.1:p.Pro358Ser
|
|
XM_024448521.1:c.2932C>T
|
XP_024304289.1:p.Pro978Ser
|
|
XR_001747870.1:n.3757C>T
|
|
|
XR_001747872.1:n.3103C>T
|
|
|
XR_001747873.1:n.3417C>T
|
|
|
NM_001301089.2:c.826C>T
|
NP_001288018.1:p.Pro276Ser
|
|
NM_001347918.2:c.2566C>T
|
NP_001334847.2:p.Pro856Ser
|
|
NM_001347919.2:c.2574-983C>T
|
NP_001334848.2:n.2574-983C>T
|
|
NM_001347920.2:c.*21082C>T
|
NP_001334849.2:n.*21082C>T
|
|
NM_001347922.2:c.1015C>T
|
NP_001334851.2:p.Pro339Ser
|
|
NM_001347923.2:c.961C>T
|
NP_001334852.2:p.Pro321Ser
|
|
NM_001347924.2:c.706C>T
|
NP_001334853.1:p.Pro236Ser
|
|
NM_001347925.2:c.652C>T
|
NP_001334854.1:p.Pro218Ser
|
|
NM_001347926.2:c.714-983C>T
|
NP_001334855.1:n.714-983C>T
|
|
NM_001347927.2:c.406C>T
|
NP_001334856.1:p.Pro136Ser
|
|
NM_014758.3:c.2686C>T
MANE Select
|
NP_055573.3:p.Pro896Ser
|
|
NR_144939.2:n.3311C>T
|
|
|