ENST00000373344.11:c.6218-139A>T
MANE Select
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ENSP00000362441.4:n.6218-139A>T
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ENST00000636152.1:n.53-139A>T
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ENST00000675732.1:c.1316-139A>T
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ENSP00000502598.1:n.1316-139A>T
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ENST00000373344.9:c.6218-139A>T
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ENSP00000362441.4:n.6218-139A>T
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ENST00000395603.7:c.6104-139A>T
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ENSP00000378967.3:n.6104-139A>T
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ENST00000480283.5:c.*5846-139A>T
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ENSP00000480196.1:n.*5846-139A>T
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ENST00000623316.1:c.702-139A>T
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ENST00000623706.3:n.3288-139A>T
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NM_000489.4:c.6218-139A>T
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NP_000480.3:n.6218-139A>T
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NM_138270.3:c.6104-139A>T
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NP_612114.2:n.6104-139A>T
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XM_005262153.3:c.6215-139A>T
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XP_005262210.2:n.6215-139A>T
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XM_005262154.3:c.6131-139A>T
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XP_005262211.2:n.6131-139A>T
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XM_005262155.3:c.6101-139A>T
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XP_005262212.2:n.6101-139A>T
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XM_005262156.3:c.6053-139A>T
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XP_005262213.2:n.6053-139A>T
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XM_005262157.3:c.6014-139A>T
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XP_005262214.2:n.6014-139A>T
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XM_006724666.2:c.6101-139A>T
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XP_006724729.1:n.6101-139A>T
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XM_006724667.2:c.5939-139A>T
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XP_006724730.1:n.5939-139A>T
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XR_938400.1:n.6560-139A>T
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NM_000489.5:c.6218-139A>T
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NP_000480.3:n.6218-139A>T
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XM_005262153.5:c.6215-139A>T
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XP_005262210.2:n.6215-139A>T
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XM_005262154.5:c.6131-139A>T
|
XP_005262211.2:n.6131-139A>T
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XM_005262155.4:c.6101-139A>T
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XP_005262212.2:n.6101-139A>T
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XM_005262156.4:c.6053-139A>T
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XP_005262213.2:n.6053-139A>T
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XM_005262157.5:c.6014-139A>T
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XP_005262214.2:n.6014-139A>T
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XM_006724666.4:c.6101-139A>T
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XP_006724729.1:n.6101-139A>T
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XM_006724667.3:c.5939-139A>T
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XP_006724730.1:n.5939-139A>T
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|
XM_017029601.2:c.6128-139A>T
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XP_016885090.1:n.6128-139A>T
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XM_017029602.1:c.6098-139A>T
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XP_016885091.1:n.6098-139A>T
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XM_017029603.1:c.6050-139A>T
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XP_016885092.1:n.6050-139A>T
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XM_017029604.2:c.6017-139A>T
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XP_016885093.1:n.6017-139A>T
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XM_017029605.1:c.6014-139A>T
|
XP_016885094.1:n.6014-139A>T
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XM_017029606.2:c.5987-139A>T
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XP_016885095.1:n.5987-139A>T
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|
XM_017029607.2:c.5984-139A>T
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XP_016885096.1:n.5984-139A>T
|
|
XM_017029608.2:c.5936-139A>T
|
XP_016885097.1:n.5936-139A>T
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|
XM_017029609.1:c.5900-139A>T
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XP_016885098.1:n.5900-139A>T
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|
XM_017029610.1:c.5897-139A>T
|
XP_016885099.1:n.5897-139A>T
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XM_017029611.1:c.5852-139A>T
|
XP_016885100.1:n.5852-139A>T
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XR_001755700.2:n.6517-139A>T
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NM_138270.4:c.6104-139A>T
|
NP_612114.2:n.6104-139A>T
|
|
NM_000489.6:c.6218-139A>T
MANE Select
|
NP_000480.3:n.6218-139A>T
|
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NM_138270.5:c.6104-139A>T
|
NP_612114.2:n.6104-139A>T
|
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