ENST00000370862.4:c.762+5498G>A
MANE Select
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ENSP00000359899.3:n.762+5498G>A
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ENST00000370862.3:c.762+5498G>A
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ENSP00000359899.3:n.762+5498G>A
|
|
ENST00000615358.4:c.762+5498G>A
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ENSP00000477548.1:n.762+5498G>A
|
|
NM_001526.3:c.762+5498G>A
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NP_001517.2:n.762+5498G>A
|
|
XM_011514542.1:c.567+5498G>A
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XP_011512844.1:n.567+5498G>A
|
|
NM_001526.4:c.762+5498G>A
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NP_001517.2:n.762+5498G>A
|
|
XM_017010798.1:c.762+5498G>A
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XP_016866287.1:n.762+5498G>A
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|
NM_001384272.1:c.762+5498G>A
MANE Select
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NP_001371201.1:n.762+5498G>A
|
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NM_001526.5:c.762+5498G>A
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NP_001517.2:n.762+5498G>A
|
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