ENST00000373344.11:c.4369G>C
MANE Select
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ENSP00000362441.4:p.Glu1457Gln
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ENST00000373344.9:c.4369G>C
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ENSP00000362441.4:p.Glu1457Gln
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ENST00000395603.7:c.4255G>C
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ENSP00000378967.3:p.Glu1419Gln
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ENST00000480283.5:c.*3997G>C
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ENSP00000480196.1:n.*3997G>C
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NM_000489.4:c.4369G>C
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NP_000480.3:p.Glu1457Gln
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NM_138270.3:c.4255G>C
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NP_612114.2:p.Glu1419Gln
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XM_005262153.3:c.4366G>C
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XP_005262210.2:p.Glu1456Gln
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XM_005262154.3:c.4282G>C
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XP_005262211.2:p.Glu1428Gln
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XM_005262155.3:c.4252G>C
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XP_005262212.2:p.Glu1418Gln
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|
XM_005262156.3:c.4204G>C
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XP_005262213.2:p.Glu1402Gln
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XM_005262157.3:c.4165G>C
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XP_005262214.2:p.Glu1389Gln
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XM_006724666.2:c.4252G>C
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XP_006724729.1:p.Glu1418Gln
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XM_006724667.2:c.4090G>C
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XP_006724730.1:p.Glu1364Gln
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|
XM_006724668.2:c.4369G>C
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XP_006724731.1:p.Glu1457Gln
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|
XR_938400.1:n.4637G>C
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|
|
NM_000489.5:c.4369G>C
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NP_000480.3:p.Glu1457Gln
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|
XM_005262153.5:c.4366G>C
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XP_005262210.2:p.Glu1456Gln
|
|
XM_005262154.5:c.4282G>C
|
XP_005262211.2:p.Glu1428Gln
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|
XM_005262155.4:c.4252G>C
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XP_005262212.2:p.Glu1418Gln
|
|
XM_005262156.4:c.4204G>C
|
XP_005262213.2:p.Glu1402Gln
|
|
XM_005262157.5:c.4165G>C
|
XP_005262214.2:p.Glu1389Gln
|
|
XM_006724666.4:c.4252G>C
|
XP_006724729.1:p.Glu1418Gln
|
|
XM_006724667.3:c.4090G>C
|
XP_006724730.1:p.Glu1364Gln
|
|
XM_006724668.3:c.4369G>C
|
XP_006724731.1:p.Glu1457Gln
|
|
XM_017029601.2:c.4279G>C
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XP_016885090.1:p.Glu1427Gln
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|
XM_017029602.1:c.4249G>C
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XP_016885091.1:p.Glu1417Gln
|
|
XM_017029603.1:c.4201G>C
|
XP_016885092.1:p.Glu1401Gln
|
|
XM_017029604.2:c.4168G>C
|
XP_016885093.1:p.Glu1390Gln
|
|
XM_017029605.1:c.4165G>C
|
XP_016885094.1:p.Glu1389Gln
|
|
XM_017029606.2:c.4138G>C
|
XP_016885095.1:p.Glu1380Gln
|
|
XM_017029607.2:c.4135G>C
|
XP_016885096.1:p.Glu1379Gln
|
|
XM_017029608.2:c.4087G>C
|
XP_016885097.1:p.Glu1363Gln
|
|
XM_017029609.1:c.4051G>C
|
XP_016885098.1:p.Glu1351Gln
|
|
XM_017029610.1:c.4048G>C
|
XP_016885099.1:p.Glu1350Gln
|
|
XM_017029611.1:c.4003G>C
|
XP_016885100.1:p.Glu1335Gln
|
|
XR_001755700.2:n.4594G>C
|
|
|
NM_138270.4:c.4255G>C
|
NP_612114.2:p.Glu1419Gln
|
|
NM_000489.6:c.4369G>C
MANE Select
|
NP_000480.3:p.Glu1457Gln
|
|
NM_138270.5:c.4255G>C
|
NP_612114.2:p.Glu1419Gln
|
|