NM_006736.6:c.825T>A
MANE Select
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NP_006727.2:p.Gly275=
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ENST00000336576.10:c.825T>A
MANE Select
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ENSP00000338019.5:p.Gly275=
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NM_001039550.1:c.823+2T>A
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NP_001034639.1:n.823+2T>A
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NM_001039550.2:c.823+2T>A
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NP_001034639.1:n.823+2T>A
|
NM_006736.5:c.825T>A
|
NP_006727.2:p.Gly275=
|
ENST00000336576.9:c.825T>A
|
ENSP00000338019.5:p.Gly275=
|
ENST00000392086.8:c.823+2T>A
|
ENSP00000375936.4:n.823+2T>A
|
ENST00000392087.6:c.732T>A
|
ENSP00000375937.2:p.Gly244=
|
ENST00000472019.5:n.566+2T>A
|
|
ENST00000473750.5:n.612T>A
|
|
ENST00000476254.1:n.449T>A
|
|
ENST00000477917.5:n.2429T>A
|
|
ENST00000684599.1:n.1032T>A
|
|