ENST00000251810.8:c.*63G>T
MANE Select
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ENSP00000251810.3:n.*63G>T
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ENST00000251810.7:c.*63G>T
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ENSP00000251810.3:n.*63G>T
|
|
ENST00000395910.6:n.506G>T
|
|
|
ENST00000522368.5:c.1288G>T
|
|
|
ENST00000621845.1:c.*63G>T
|
ENSP00000484318.1:n.*63G>T
|
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NM_001172477.1:c.*63G>T , LRG_788t1:c.*63G>T
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NP_001165948.1:n.*63G>T
|
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NM_001172478.1:c.*63G>T
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NP_001165949.1:n.*63G>T
|
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NM_015713.4:c.*63G>T , LRG_788t2:c.*63G>T
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NP_056528.2:n.*63G>T
|
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NM_001172478.2:c.*63G>T
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NP_001165949.1:n.*63G>T
|
|
NM_015713.5:c.*63G>T
MANE Select
|
NP_056528.2:n.*63G>T
|
|