ENST00000269980.7:c.375+126A>G
MANE Select
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ENSP00000269980.2:n.375+126A>G
|
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ENST00000269980.6:c.375+126A>G
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ENSP00000269980.2:n.375+126A>G
|
|
ENST00000457836.6:c.309+126A>G
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ENSP00000416000.2:n.309+126A>G
|
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ENST00000538423.5:n.501+126A>G
|
|
|
ENST00000540732.3:c.477+126A>G
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ENSP00000443246.1:n.477+126A>G
|
|
ENST00000541315.1:c.182+126A>G
|
|
|
ENST00000542943.5:c.288+319A>G
|
ENSP00000440345.1:n.288+319A>G
|
|
ENST00000595085.5:c.375+126A>G
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ENSP00000471150.2:n.375+126A>G
|
|
NM_000709.3:c.375+126A>G
|
NP_000700.1:n.375+126A>G
|
|
NM_001164783.1:c.375+126A>G
|
NP_001158255.1:n.375+126A>G
|
|
NM_000709.4:c.375+126A>G
MANE Select
|
NP_000700.1:n.375+126A>G
|
|
NM_001164783.2:c.375+126A>G
|
NP_001158255.1:n.375+126A>G
|
|