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ENST00000255674.11:c.3278C=
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ENSP00000255674.7:p.Thr1093=
|
|
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ENST00000638251.1:c.*1270C=
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ENSP00000491968.1:n.*1270C=
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ENST00000638298.1:c.267C=
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ENST00000639128.1:n.824C=
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ENST00000640376.1:c.2624+751C=
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ENSP00000491654.1:n.2624+751C=
|
|
|
ENST00000640408.1:n.3710C=
|
|
|
|
ENST00000640769.2:c.3278C=
MANE Select
|
ENSP00000491507.1:p.Thr1093=
|
|
|
ENST00000640931.1:c.499C=
|
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ENST00000677824.1:c.783-5907C=
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ENSP00000504646.1:n.783-5907C=
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ENST00000679113.1:c.500C=
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ENSP00000504487.1:p.Thr167=
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|
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ENST00000255674.10:c.3278C=
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ENSP00000255674.6:p.Thr1093=
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ENST00000581161.5:c.*1592C=
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ENSP00000462926.1:n.*1592C=
|
|
|
ENST00000583043.5:c.2559C=
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ENSP00000462733.1:n.2559C=
|
|
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NM_173630.3:c.3278C=
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NP_775901.3:p.Thr1093=
|
|
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XM_005266679.1:c.542C=
|
XP_005266736.1:p.Thr181=
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|
|
XM_006722434.2:c.3281C=
|
XP_006722497.1:p.Thr1094=
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XM_006722435.2:c.3281C=
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XP_006722498.1:p.Thr1094=
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XM_011525902.1:c.3146+751C=
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XP_011524204.1:n.3146+751C=
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XM_011525903.1:c.2958-5907C=
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XP_011524205.1:n.2958-5907C=
|
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XM_011525904.1:c.3281C=
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XP_011524206.1:p.Thr1094=
|
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XM_011525905.1:c.3281C=
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XP_011524207.1:p.Thr1094=
|
|
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XM_011525906.1:c.1781C=
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XP_011524208.1:p.Thr594=
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XM_011525907.1:c.3281C=
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XP_011524209.1:p.Thr1094=
|
|
|
XM_011525908.1:c.3281C=
|
XP_011524210.1:p.Thr1094=
|
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XR_430072.2:n.3319C=
|
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XR_935213.1:n.3319C=
|
|
|
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NM_001318520.1:c.542C=
|
NP_001305449.1:p.Thr181=
|
|
|
XM_006722434.3:c.3281C=
|
XP_006722497.1:p.Thr1094=
|
|
|
XM_006722435.3:c.3281C=
|
XP_006722498.1:p.Thr1094=
|
|
|
XM_011525902.2:c.3146+751C=
|
XP_011524204.1:n.3146+751C=
|
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XM_011525903.2:c.2958-5907C=
|
XP_011524205.1:n.2958-5907C=
|
|
|
XM_011525904.3:c.3281C=
|
XP_011524206.1:p.Thr1094=
|
|
|
XM_011525905.2:c.3281C=
|
XP_011524207.1:p.Thr1094=
|
|
|
XM_011525906.2:c.1781C=
|
XP_011524208.1:p.Thr594=
|
|
|
XM_011525907.2:c.3281C=
|
XP_011524209.1:p.Thr1094=
|
|
|
XM_011525908.3:c.3281C=
|
XP_011524210.1:p.Thr1094=
|
|
|
XM_017025693.1:c.3143+751C=
|
XP_016881182.1:n.3143+751C=
|
|
|
XM_017025694.1:c.2639C=
|
XP_016881183.1:p.Thr880=
|
|
|
XM_017025695.1:c.2216C=
|
XP_016881184.1:p.Thr739=
|
|
|
XM_017025696.1:c.1172C=
|
XP_016881185.1:p.Thr391=
|
|
|
XM_024451139.1:c.2501C=
|
XP_024306907.1:p.Thr834=
|
|
|
XM_024451140.1:c.2501C=
|
XP_024306908.1:p.Thr834=
|
|
|
XR_430072.3:n.3349C=
|
|
|
|
XR_935213.2:n.3349C=
|
|
|
|
NM_001318520.2:c.542C=
|
NP_001305449.1:p.Thr181=
|
|
|
NM_173630.4:c.3278C=
MANE Select
|
NP_775901.3:p.Thr1093=
|
|
