ENST00000241436.9:c.2517A>C
MANE Select
|
ENSP00000241436.4:p.Thr839=
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ENST00000241436.8:c.2517A>C
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ENSP00000241436.4:p.Thr839=
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ENST00000502567.1:n.362A>C
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ENST00000503479.6:c.*1040A>C
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ENSP00000421997.2:n.*1040A>C
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ENST00000504026.5:c.1388A>C
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ENSP00000425075.1:n.1388A>C
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ENST00000505069.1:n.97A>C
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ENST00000505975.5:c.2631A>C
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ENSP00000424859.1:n.2631A>C
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ENST00000506928.5:n.2640A>C
|
|
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ENST00000508526.5:c.1923A>C
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ENSP00000426853.1:p.Thr641=
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ENST00000509126.2:c.2345A>C
|
ENSP00000423532.1:n.2345A>C
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ENST00000510815.6:c.*1040A>C
|
ENSP00000422094.2:n.*1040A>C
|
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ENST00000511527.5:c.1502A>C
|
ENSP00000420997.1:n.1502A>C
|
|
ENST00000514141.5:c.*1136A>C
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ENSP00000423526.1:n.*1136A>C
|
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NM_016218.2:c.2517A>C
|
NP_057302.1:p.Thr839=
|
|
XM_005248534.3:c.2559A>C
|
XP_005248591.1:p.Thr853=
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XM_006714652.2:c.1272A>C
|
XP_006714715.1:p.Thr424=
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XM_011543463.1:c.2559A>C
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XP_011541765.1:p.Thr853=
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XM_011543464.1:c.2559A>C
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XP_011541766.1:p.Thr853=
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XM_011543465.1:c.2559A>C
|
XP_011541767.1:p.Thr853=
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XM_011543466.1:c.2559A>C
|
XP_011541768.1:p.Thr853=
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XM_011543467.1:c.2289A>C
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XP_011541769.1:p.Thr763=
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XR_241784.1:n.2525A>C
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XR_948273.1:n.2709A>C
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NM_001345921.1:c.2319A>C
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NP_001332850.1:p.Thr773=
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NM_001345922.1:c.2247A>C
|
NP_001332851.1:p.Thr749=
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NM_016218.3:c.2517A>C
|
NP_057302.1:p.Thr839=
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|
NR_144315.1:n.2523A>C
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|
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XM_005248534.5:c.2559A>C
|
XP_005248591.1:p.Thr853=
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|
XM_006714652.4:c.1272A>C
|
XP_006714715.1:p.Thr424=
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|
XM_011543463.3:c.2559A>C
|
XP_011541765.1:p.Thr853=
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XM_011543464.3:c.2559A>C
|
XP_011541766.1:p.Thr853=
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XM_011543467.3:c.2289A>C
|
XP_011541769.1:p.Thr763=
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XM_017009559.2:c.2517A>C
|
XP_016865048.1:p.Thr839=
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XM_017009560.2:c.2517A>C
|
XP_016865049.1:p.Thr839=
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XM_017009561.2:c.2361A>C
|
XP_016865050.1:p.Thr787=
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XM_017009563.2:c.2247A>C
|
XP_016865052.1:p.Thr749=
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XR_001742105.2:n.3007A>C
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XR_001742107.2:n.3091A>C
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XR_001742108.2:n.2625A>C
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XR_241784.3:n.3049A>C
|
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XR_948273.3:n.2709A>C
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NM_001345921.2:c.2319A>C
|
NP_001332850.1:p.Thr773=
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|
NM_001345922.2:c.2247A>C
|
NP_001332851.1:p.Thr749=
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|
NM_001387110.2:c.2508A>C
|
NP_001374039.1:p.Thr836=
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|
NM_001387111.2:c.2559A>C
|
NP_001374040.1:p.Thr853=
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|
NM_001387113.2:c.2517A>C
|
NP_001374042.1:p.Thr839=
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|
NM_016218.5:c.2517A>C
|
NP_057302.1:p.Thr839=
|
|
NR_144315.2:n.2382A>C
|
|
|
NR_170559.2:n.2371A>C
|
|
|
NR_170560.2:n.2603A>C
|
|
|
NM_001345921.3:c.2319A>C
|
NP_001332850.1:p.Thr773=
|
|
NM_001345922.3:c.2247A>C
|
NP_001332851.1:p.Thr749=
|
|
NM_001387110.3:c.2508A>C
|
NP_001374039.1:p.Thr836=
|
|
NM_001387111.3:c.2559A>C
|
NP_001374040.1:p.Thr853=
|
|
NM_001387113.3:c.2517A>C
|
NP_001374042.1:p.Thr839=
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|
NM_001395893.1:c.2247A>C
|
NP_001382822.1:p.Thr749=
|
|
NM_001395894.1:c.2559A>C
|
NP_001382823.1:p.Thr853=
|
|
NM_001395897.1:c.2556A>C
|
NP_001382826.1:p.Thr852=
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|
NM_001395899.1:c.2364A>C
|
NP_001382828.1:p.Thr788=
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|
NM_001395900.1:c.2319A>C
|
NP_001382829.1:p.Thr773=
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|
NM_001395901.1:c.2277A>C
|
NP_001382830.1:p.Thr759=
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|
NM_001395902.1:c.2247A>C
|
NP_001382831.1:p.Thr749=
|
|
NM_016218.6:c.2517A>C
MANE Select
|
NP_057302.1:p.Thr839=
|
|
NR_144315.3:n.2382A>C
|
|
|
NR_170559.3:n.2371A>C
|
|
|
NR_170560.3:n.2603A>C
|
|
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