ENST00000248846.10:c.3536C>T
MANE Select
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ENSP00000248846.5:p.Ala1179Val
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ENST00000248846.9:c.3536C>T
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ENSP00000248846.5:p.Ala1179Val
|
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ENST00000439308.6:c.3536C>T
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ENSP00000397387.2:p.Ala1179Val
|
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ENST00000491449.5:n.1843C>T
|
|
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ENST00000498611.5:n.3617+452C>T
|
|
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NM_020461.3:c.3536C>T
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NP_065194.2:p.Ala1179Val
|
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XR_938347.1:n.4101C>T
|
|
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XR_938348.1:n.3050-808C>T
|
|
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XR_001755343.2:n.4105C>T
|
|
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XR_001755344.2:n.4105C>T
|
|
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XR_002958720.1:n.3054-808C>T
|
|
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XR_938347.2:n.4105C>T
|
|
|
NM_020461.4:c.3536C>T
MANE Select
|
NP_065194.3:p.Ala1179Val
|
|