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NM_000489.6:c.1262A>G
MANE Select
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NP_000480.3:p.Asp421Gly
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ENST00000373344.11:c.1262A>G
MANE Select
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ENSP00000362441.4:p.Asp421Gly
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NM_000489.4:c.1262A>G
|
NP_000480.3:p.Asp421Gly
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NM_000489.5:c.1262A>G
|
NP_000480.3:p.Asp421Gly
|
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NM_138270.3:c.1148A>G
|
NP_612114.2:p.Asp383Gly
|
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NM_138270.4:c.1148A>G
|
NP_612114.2:p.Asp383Gly
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NM_138270.5:c.1148A>G
|
NP_612114.2:p.Asp383Gly
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ENST00000373344.9:c.1262A>G
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ENSP00000362441.4:p.Asp421Gly
|
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ENST00000395603.7:c.1148A>G
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ENSP00000378967.3:p.Asp383Gly
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ENST00000480283.5:c.*890A>G
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ENSP00000480196.1:n.*890A>G
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ENST00000623321.3:c.1097A>G
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ENSP00000485127.1:p.Asp366Gly
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ENST00000624032.3:c.1262A>G
|
ENSP00000485253.1:p.Asp421Gly
|
|
ENST00000624166.3:c.1145A>G
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ENSP00000485103.1:p.Asp382Gly
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XM_005262153.3:c.1259A>G
|
XP_005262210.2:p.Asp420Gly
|
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XM_005262153.5:c.1259A>G
|
XP_005262210.2:p.Asp420Gly
|
|
XM_005262154.3:c.1262A>G
|
XP_005262211.2:p.Asp421Gly
|
|
XM_005262154.5:c.1262A>G
|
XP_005262211.2:p.Asp421Gly
|
|
XM_005262155.3:c.1145A>G
|
XP_005262212.2:p.Asp382Gly
|
|
XM_005262155.4:c.1145A>G
|
XP_005262212.2:p.Asp382Gly
|
|
XM_005262156.3:c.1097A>G
|
XP_005262213.2:p.Asp366Gly
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|
XM_005262156.4:c.1097A>G
|
XP_005262213.2:p.Asp366Gly
|
|
XM_005262157.3:c.1145A>G
|
XP_005262214.2:p.Asp382Gly
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|
XM_005262157.5:c.1145A>G
|
XP_005262214.2:p.Asp382Gly
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XM_006724666.2:c.1145A>G
|
XP_006724729.1:p.Asp382Gly
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XM_006724666.4:c.1145A>G
|
XP_006724729.1:p.Asp382Gly
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XM_006724667.2:c.983A>G
|
XP_006724730.1:p.Asp328Gly
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|
XM_006724667.3:c.983A>G
|
XP_006724730.1:p.Asp328Gly
|
|
XM_006724668.2:c.1262A>G
|
XP_006724731.1:p.Asp421Gly
|
|
XM_006724668.3:c.1262A>G
|
XP_006724731.1:p.Asp421Gly
|
|
XM_017029601.2:c.1259A>G
|
XP_016885090.1:p.Asp420Gly
|
|
XM_017029602.1:c.1142A>G
|
XP_016885091.1:p.Asp381Gly
|
|
XM_017029603.1:c.1094A>G
|
XP_016885092.1:p.Asp365Gly
|
|
XM_017029604.2:c.1148A>G
|
XP_016885093.1:p.Asp383Gly
|
|
XM_017029605.1:c.1145A>G
|
XP_016885094.1:p.Asp382Gly
|
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XM_017029606.2:c.1031A>G
|
XP_016885095.1:p.Asp344Gly
|
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XM_017029607.2:c.1028A>G
|
XP_016885096.1:p.Asp343Gly
|
|
XM_017029608.2:c.980A>G
|
XP_016885097.1:p.Asp327Gly
|
|
XM_017029609.1:c.1031A>G
|
XP_016885098.1:p.Asp344Gly
|
|
XM_017029610.1:c.1028A>G
|
XP_016885099.1:p.Asp343Gly
|
|
XM_017029611.1:c.983A>G
|
XP_016885100.1:p.Asp328Gly
|
|
XR_001755700.2:n.1487A>G
|
|
|
XR_938400.1:n.1530A>G
|
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