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ENST00000389817.8:c.2508A>G
MANE Select
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NM_000352.4:c.2508A>G
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NP_000343.2:p.Arg836=
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NM_001287174.1:c.2511A>G
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NP_001274103.1:p.Arg837=
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XR_930892.1:n.2574A>G
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XM_017018204.1:c.465A>G
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XM_024448668.1:c.876A>G
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XR_002957189.1:n.2649A>G
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NM_000352.6:c.2508A>G
MANE Select
|
NP_000343.2:p.Arg836=
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NM_001287174.2:c.2511A>G
|
NP_001274103.1:p.Arg837=
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NM_001351296.2:c.2508A>G
|
NP_001338225.1:p.Arg836=
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NM_001351297.2:c.2505A>G
|
NP_001338226.1:p.Arg835=
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NR_147094.2:n.2577A>G
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NM_001287174.3:c.2511A>G
|
NP_001274103.1:p.Arg837=
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|
