ENST00000681320.1:c.7975G>T
MANE Select
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ENSP00000506558.1:p.Gly2659Ter
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ENST00000328333.12:c.7975G>T
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ENSP00000332371.8:p.Gly2659Ter
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ENST00000459756.5:n.798G>T
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ENST00000487017.5:n.4614G>T
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NM_000094.3:c.7975G>T , LRG_286t1:c.7975G>T
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NP_000085.1:p.Gly2659Ter
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XM_011533336.1:c.8002G>T
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XP_011531638.1:p.Gly2668Ter
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XM_011533337.1:c.7975G>T
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XP_011531639.1:p.Gly2659Ter
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XM_011533338.1:c.7942G>T
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XP_011531640.1:p.Gly2648Ter
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XR_940369.1:n.8038G>T
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XR_940370.1:n.8038G>T
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XR_940371.1:n.8038G>T
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XM_017005688.1:c.7915G>T
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XP_016861177.1:p.Gly2639Ter
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XR_001740003.1:n.8011G>T
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XR_001740004.1:n.8011G>T
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XR_001740005.1:n.8011G>T
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NM_000094.4:c.7975G>T
MANE Select
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NP_000085.1:p.Gly2659Ter
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