ENST00000248846.10:c.3857C>G
MANE Select
|
ENSP00000248846.5:p.Ala1286Gly
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ENST00000248846.9:c.3857C>G
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ENSP00000248846.5:p.Ala1286Gly
|
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ENST00000439308.6:c.3857C>G
|
ENSP00000397387.2:p.Ala1286Gly
|
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ENST00000491449.5:n.2164C>G
|
|
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ENST00000498611.5:n.3618-487C>G
|
|
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NM_020461.3:c.3857C>G
|
NP_065194.2:p.Ala1286Gly
|
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XR_938347.1:n.4422C>G
|
|
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XR_938348.1:n.3050-487C>G
|
|
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XR_001755343.2:n.4426C>G
|
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XR_001755344.2:n.4426C>G
|
|
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XR_002958720.1:n.3054-487C>G
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|
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XR_938347.2:n.4426C>G
|
|
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NM_020461.4:c.3857C>G
MANE Select
|
NP_065194.3:p.Ala1286Gly
|
|