ENST00000373344.11:c.4381G>C
MANE Select
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ENSP00000362441.4:p.Glu1461Gln
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ENST00000373344.9:c.4381G>C
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ENSP00000362441.4:p.Glu1461Gln
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ENST00000395603.7:c.4267G>C
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ENSP00000378967.3:p.Glu1423Gln
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ENST00000480283.5:c.*4009G>C
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ENSP00000480196.1:n.*4009G>C
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NM_000489.4:c.4381G>C
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NP_000480.3:p.Glu1461Gln
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NM_138270.3:c.4267G>C
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NP_612114.2:p.Glu1423Gln
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XM_005262153.3:c.4378G>C
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XP_005262210.2:p.Glu1460Gln
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XM_005262154.3:c.4294G>C
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XP_005262211.2:p.Glu1432Gln
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XM_005262155.3:c.4264G>C
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XP_005262212.2:p.Glu1422Gln
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|
XM_005262156.3:c.4216G>C
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XP_005262213.2:p.Glu1406Gln
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XM_005262157.3:c.4177G>C
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XP_005262214.2:p.Glu1393Gln
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XM_006724666.2:c.4264G>C
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XP_006724729.1:p.Glu1422Gln
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XM_006724667.2:c.4102G>C
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XP_006724730.1:p.Glu1368Gln
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|
XM_006724668.2:c.4381G>C
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XP_006724731.1:p.Glu1461Gln
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|
XR_938400.1:n.4649G>C
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|
|
NM_000489.5:c.4381G>C
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NP_000480.3:p.Glu1461Gln
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|
XM_005262153.5:c.4378G>C
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XP_005262210.2:p.Glu1460Gln
|
|
XM_005262154.5:c.4294G>C
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XP_005262211.2:p.Glu1432Gln
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|
XM_005262155.4:c.4264G>C
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XP_005262212.2:p.Glu1422Gln
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|
XM_005262156.4:c.4216G>C
|
XP_005262213.2:p.Glu1406Gln
|
|
XM_005262157.5:c.4177G>C
|
XP_005262214.2:p.Glu1393Gln
|
|
XM_006724666.4:c.4264G>C
|
XP_006724729.1:p.Glu1422Gln
|
|
XM_006724667.3:c.4102G>C
|
XP_006724730.1:p.Glu1368Gln
|
|
XM_006724668.3:c.4381G>C
|
XP_006724731.1:p.Glu1461Gln
|
|
XM_017029601.2:c.4291G>C
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XP_016885090.1:p.Glu1431Gln
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|
XM_017029602.1:c.4261G>C
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XP_016885091.1:p.Glu1421Gln
|
|
XM_017029603.1:c.4213G>C
|
XP_016885092.1:p.Glu1405Gln
|
|
XM_017029604.2:c.4180G>C
|
XP_016885093.1:p.Glu1394Gln
|
|
XM_017029605.1:c.4177G>C
|
XP_016885094.1:p.Glu1393Gln
|
|
XM_017029606.2:c.4150G>C
|
XP_016885095.1:p.Glu1384Gln
|
|
XM_017029607.2:c.4147G>C
|
XP_016885096.1:p.Glu1383Gln
|
|
XM_017029608.2:c.4099G>C
|
XP_016885097.1:p.Glu1367Gln
|
|
XM_017029609.1:c.4063G>C
|
XP_016885098.1:p.Glu1355Gln
|
|
XM_017029610.1:c.4060G>C
|
XP_016885099.1:p.Glu1354Gln
|
|
XM_017029611.1:c.4015G>C
|
XP_016885100.1:p.Glu1339Gln
|
|
XR_001755700.2:n.4606G>C
|
|
|
NM_138270.4:c.4267G>C
|
NP_612114.2:p.Glu1423Gln
|
|
NM_000489.6:c.4381G>C
MANE Select
|
NP_000480.3:p.Glu1461Gln
|
|
NM_138270.5:c.4267G>C
|
NP_612114.2:p.Glu1423Gln
|
|