ENST00000265909.9:c.2738G=
MANE Select
|
ENSP00000265909.4:p.Ser913=
|
|
ENST00000265909.8:c.2738G=
|
ENSP00000265909.4:p.Ser913=
|
|
ENST00000426933.6:c.242G=
|
ENSP00000413345.2:p.Ser81=
|
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ENST00000526579.5:n.178-931G=
|
|
|
ENST00000527116.5:n.500G=
|
|
|
ENST00000528555.5:c.878G=
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ENSP00000435122.1:p.Ser293=
|
|
ENST00000530330.1:n.474G=
|
|
|
ENST00000530356.5:c.878G=
|
ENSP00000432307.1:p.Ser293=
|
|
ENST00000533318.5:n.1098G=
|
|
|
ENST00000534726.5:c.458G=
|
ENSP00000433699.1:p.Ser153=
|
|
NM_001301089.1:c.878G=
|
NP_001288018.1:p.Ser293=
|
|
NM_014758.2:c.2738G=
|
NP_055573.2:p.Ser913=
|
|
XM_005271546.3:c.2574-931G=
|
XP_005271603.1:n.2574-931G=
|
|
XM_011542819.1:c.2984G=
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XP_011541121.1:p.Ser995=
|
|
XM_011542820.1:c.2972G=
|
XP_011541122.1:p.Ser991=
|
|
XM_011542821.1:c.2864G=
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XP_011541123.1:p.Ser955=
|
|
XM_011542824.1:c.2102G=
|
XP_011541126.1:p.Ser701=
|
|
XM_011542825.1:c.1259G=
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XP_011541127.1:p.Ser420=
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|
XM_011542826.1:c.1124G=
|
XP_011541128.1:p.Ser375=
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|
XM_011542827.1:c.1004G=
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XP_011541129.1:p.Ser335=
|
|
NM_001347918.1:c.2618G=
|
NP_001334847.1:p.Ser873=
|
|
NM_001347919.1:c.2574-931G=
|
NP_001334848.1:n.2574-931G=
|
|
NM_001347922.1:c.1067G=
|
NP_001334851.1:p.Ser356=
|
|
NM_001347923.1:c.1013G=
|
NP_001334852.1:p.Ser338=
|
|
NM_001347924.1:c.758G=
|
NP_001334853.1:p.Ser253=
|
|
NM_001347925.1:c.704G=
|
NP_001334854.1:p.Ser235=
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|
NM_001347926.1:c.714-931G=
|
NP_001334855.1:n.714-931G=
|
|
NM_001347927.1:c.458G=
|
NP_001334856.1:p.Ser153=
|
|
NR_144939.1:n.3371G=
|
|
|
XM_011542820.2:c.2972G=
|
XP_011541122.1:p.Ser991=
|
|
XM_011542821.3:c.2864G=
|
XP_011541123.1:p.Ser955=
|
|
XM_011542824.2:c.2102G=
|
XP_011541126.1:p.Ser701=
|
|
XM_011542825.2:c.1259G=
|
XP_011541127.1:p.Ser420=
|
|
XM_011542826.2:c.1124G=
|
XP_011541128.1:p.Ser375=
|
|
XM_024448521.1:c.2984G=
|
XP_024304289.1:p.Ser995=
|
|
XR_001747870.1:n.3809G=
|
|
|
XR_001747872.1:n.3155G=
|
|
|
XR_001747873.1:n.3469G=
|
|
|
NM_001301089.2:c.878G=
|
NP_001288018.1:p.Ser293=
|
|
NM_001347918.2:c.2618G=
|
NP_001334847.2:p.Ser873=
|
|
NM_001347919.2:c.2574-931G=
|
NP_001334848.2:n.2574-931G=
|
|
NM_001347920.2:c.*21134G=
|
NP_001334849.2:n.*21134G=
|
|
NM_001347922.2:c.1067G=
|
NP_001334851.2:p.Ser356=
|
|
NM_001347923.2:c.1013G=
|
NP_001334852.2:p.Ser338=
|
|
NM_001347924.2:c.758G=
|
NP_001334853.1:p.Ser253=
|
|
NM_001347925.2:c.704G=
|
NP_001334854.1:p.Ser235=
|
|
NM_001347926.2:c.714-931G=
|
NP_001334855.1:n.714-931G=
|
|
NM_001347927.2:c.458G=
|
NP_001334856.1:p.Ser153=
|
|
NM_014758.3:c.2738G=
MANE Select
|
NP_055573.3:p.Ser913=
|
|
NR_144939.2:n.3363G=
|
|
|