ENST00000255674.11:c.3176A>G
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ENSP00000255674.7:p.Asp1059Gly
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ENST00000638251.1:c.*1168A>G
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ENSP00000491968.1:n.*1168A>G
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ENST00000638298.1:c.165A>G
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ENST00000639128.1:n.722A>G
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|
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ENST00000640376.1:c.2624+649A>G
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ENSP00000491654.1:n.2624+649A>G
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ENST00000640408.1:n.3608A>G
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|
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ENST00000640769.2:c.3176A>G
MANE Select
|
ENSP00000491507.1:p.Asp1059Gly
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ENST00000640931.1:c.397A>G
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ENST00000677824.1:c.783-6009A>G
|
ENSP00000504646.1:n.783-6009A>G
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ENST00000679113.1:c.398A>G
|
ENSP00000504487.1:p.Asp133Gly
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ENST00000255674.10:c.3176A>G
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ENSP00000255674.6:p.Asp1059Gly
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|
ENST00000581161.5:c.*1490A>G
|
ENSP00000462926.1:n.*1490A>G
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ENST00000583043.5:c.2457A>G
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ENSP00000462733.1:n.2457A>G
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NM_173630.3:c.3176A>G
|
NP_775901.3:p.Asp1059Gly
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|
XM_005266679.1:c.440A>G
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XP_005266736.1:p.Asp147Gly
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XM_006722434.2:c.3179A>G
|
XP_006722497.1:p.Asp1060Gly
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|
XM_006722435.2:c.3179A>G
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XP_006722498.1:p.Asp1060Gly
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|
XM_011525902.1:c.3146+649A>G
|
XP_011524204.1:n.3146+649A>G
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|
XM_011525903.1:c.2958-6009A>G
|
XP_011524205.1:n.2958-6009A>G
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|
XM_011525904.1:c.3179A>G
|
XP_011524206.1:p.Asp1060Gly
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|
XM_011525905.1:c.3179A>G
|
XP_011524207.1:p.Asp1060Gly
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|
XM_011525906.1:c.1679A>G
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XP_011524208.1:p.Asp560Gly
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|
XM_011525907.1:c.3179A>G
|
XP_011524209.1:p.Asp1060Gly
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|
XM_011525908.1:c.3179A>G
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XP_011524210.1:p.Asp1060Gly
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|
XR_430072.2:n.3217A>G
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|
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XR_935213.1:n.3217A>G
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|
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NM_001318520.1:c.440A>G
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NP_001305449.1:p.Asp147Gly
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|
XM_006722434.3:c.3179A>G
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XP_006722497.1:p.Asp1060Gly
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|
XM_006722435.3:c.3179A>G
|
XP_006722498.1:p.Asp1060Gly
|
|
XM_011525902.2:c.3146+649A>G
|
XP_011524204.1:n.3146+649A>G
|
|
XM_011525903.2:c.2958-6009A>G
|
XP_011524205.1:n.2958-6009A>G
|
|
XM_011525904.3:c.3179A>G
|
XP_011524206.1:p.Asp1060Gly
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|
XM_011525905.2:c.3179A>G
|
XP_011524207.1:p.Asp1060Gly
|
|
XM_011525906.2:c.1679A>G
|
XP_011524208.1:p.Asp560Gly
|
|
XM_011525907.2:c.3179A>G
|
XP_011524209.1:p.Asp1060Gly
|
|
XM_011525908.3:c.3179A>G
|
XP_011524210.1:p.Asp1060Gly
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|
XM_017025693.1:c.3143+649A>G
|
XP_016881182.1:n.3143+649A>G
|
|
XM_017025694.1:c.2537A>G
|
XP_016881183.1:p.Asp846Gly
|
|
XM_017025695.1:c.2114A>G
|
XP_016881184.1:p.Asp705Gly
|
|
XM_017025696.1:c.1070A>G
|
XP_016881185.1:p.Asp357Gly
|
|
XM_024451139.1:c.2399A>G
|
XP_024306907.1:p.Asp800Gly
|
|
XM_024451140.1:c.2399A>G
|
XP_024306908.1:p.Asp800Gly
|
|
XR_430072.3:n.3247A>G
|
|
|
XR_935213.2:n.3247A>G
|
|
|
NM_001318520.2:c.440A>G
|
NP_001305449.1:p.Asp147Gly
|
|
NM_173630.4:c.3176A>G
MANE Select
|
NP_775901.3:p.Asp1059Gly
|
|