ENST00000681320.1:c.7815A>T
MANE Select
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ENSP00000506558.1:p.Gly2605=
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ENST00000328333.12:c.7815A>T
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ENSP00000332371.8:p.Gly2605=
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ENST00000459756.5:n.638A>T
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ENST00000487017.5:n.4454A>T
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NM_000094.3:c.7815A>T , LRG_286t1:c.7815A>T
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NP_000085.1:p.Gly2605=
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XM_011533336.1:c.7842A>T
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XP_011531638.1:p.Gly2614=
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XM_011533337.1:c.7815A>T
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XP_011531639.1:p.Gly2605=
|
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XM_011533338.1:c.7782A>T
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XP_011531640.1:p.Gly2594=
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XM_011533339.1:c.*47A>T
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XP_011531641.1:n.*47A>T
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XR_940369.1:n.7878A>T
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|
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XR_940370.1:n.7878A>T
|
|
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XR_940371.1:n.7878A>T
|
|
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XR_940372.1:n.7852A>T
|
|
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XM_017005688.1:c.7755A>T
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XP_016861177.1:p.Gly2585=
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XM_017005689.1:c.*47A>T
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XP_016861178.1:n.*47A>T
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XR_001740003.1:n.7851A>T
|
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XR_001740004.1:n.7851A>T
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XR_001740005.1:n.7851A>T
|
|
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XR_001740006.1:n.7825A>T
|
|
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NM_000094.4:c.7815A>T
MANE Select
|
NP_000085.1:p.Gly2605=
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