ENST00000251810.8:c.*116G>T
MANE Select
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ENSP00000251810.3:n.*116G>T
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ENST00000251810.7:c.*116G>T
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ENSP00000251810.3:n.*116G>T
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ENST00000395910.6:n.559G>T
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|
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ENST00000522368.5:c.1341G>T
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|
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ENST00000621845.1:c.*116G>T
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ENSP00000484318.1:n.*116G>T
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NM_001172477.1:c.*116G>T , LRG_788t1:c.*116G>T
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NP_001165948.1:n.*116G>T
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NM_001172478.1:c.*116G>T
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NP_001165949.1:n.*116G>T
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NM_015713.4:c.*116G>T , LRG_788t2:c.*116G>T
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NP_056528.2:n.*116G>T
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NM_001172478.2:c.*116G>T
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NP_001165949.1:n.*116G>T
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NM_015713.5:c.*116G>T
MANE Select
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NP_056528.2:n.*116G>T
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