ENST00000373296.8:c.701A>G
MANE Select
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ENSP00000362393.3:p.Asp234Gly
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ENST00000373294.8:c.701A>G
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ENSP00000362390.5:p.Asp234Gly
|
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ENST00000373296.7:c.701A>G
|
ENSP00000362393.3:p.Asp234Gly
|
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ENST00000626498.2:c.*313A>G
|
ENSP00000487527.1:n.*313A>G
|
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ENST00000626877.1:n.580A>G
|
|
|
NM_001109878.1:c.701A>G
|
NP_001103348.1:p.Asp234Gly
|
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NM_001109879.1:c.341A>G
|
NP_001103349.1:p.Asp114Gly
|
|
NM_001303475.1:c.341A>G
|
NP_001290404.1:p.Asp114Gly
|
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NM_016954.2:c.701A>G
|
NP_058650.1:p.Asp234Gly
|
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XM_005262136.2:c.704A>G
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XP_005262193.1:p.Asp235Gly
|
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XM_006724657.2:c.704A>G
|
XP_006724720.1:p.Asp235Gly
|
|
XM_011530972.1:c.341A>G
|
XP_011529274.1:p.Asp114Gly
|
|
NM_001109878.2:c.701A>G
MANE Select
|
NP_001103348.1:p.Asp234Gly
|
|
NM_001109879.2:c.341A>G
|
NP_001103349.1:p.Asp114Gly
|
|