ENST00000246337.9:c.504T>C
MANE Select
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ENSP00000246337.4:p.Gly168=
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ENST00000434478.6:c.558T>C
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ENSP00000404489.2:p.Gly186=
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ENST00000491773.6:c.399T>C
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ENSP00000498551.1:p.Gly133=
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ENST00000636293.1:c.504T>C
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ENSP00000490710.1:p.Gly168=
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ENST00000636836.1:c.504T>C
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ENSP00000490594.1:p.Gly168=
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ENST00000651476.1:c.399T>C
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ENSP00000498668.1:p.Gly133=
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ENST00000652165.1:c.399T>C
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ENSP00000498295.1:p.Gly133=
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ENST00000652287.1:c.441T>C
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ENSP00000498413.1:p.Gly147=
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ENST00000652514.1:c.465T>C
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ENSP00000498635.1:n.465T>C
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ENST00000246337.8:c.504T>C
|
ENSP00000246337.4:p.Gly168=
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ENST00000428106.1:c.454+147T>C
|
|
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ENST00000434478.5:c.441T>C
|
ENSP00000404489.1:p.Gly147=
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|
ENST00000460334.5:n.531T>C
|
|
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ENST00000460906.5:n.638T>C
|
|
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ENST00000462688.5:n.631T>C
|
|
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ENST00000469548.5:n.700T>C
|
|
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ENST00000473012.1:n.551T>C
|
|
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ENST00000478467.5:n.507T>C
|
|
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ENST00000486699.5:n.624T>C
|
|
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ENST00000490385.5:n.578T>C
|
|
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ENST00000491300.5:n.623T>C
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ENST00000491773.5:n.658T>C
|
|
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ENST00000494399.5:n.644T>C
|
|
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ENST00000496439.1:n.600T>C
|
|
|
NM_000374.4:c.504T>C
|
NP_000365.3:p.Gly168=
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|
NR_036510.1:n.687T>C
|
|
|
XM_005271169.1:c.288T>C
|
XP_005271226.1:p.Gly96=
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|
XM_005271170.1:c.288T>C
|
XP_005271227.1:p.Gly96=
|
|
XM_011542080.1:c.441T>C
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XP_011540382.1:p.Gly147=
|
|
XM_011542081.1:c.336T>C
|
XP_011540383.1:p.Gly112=
|
|
NM_000374.5:c.504T>C
MANE Select
|
NP_000365.3:p.Gly168=
|
|
NR_158184.1:n.585T>C
|
|
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NR_158185.1:n.535T>C
|
|
|
NR_036510.2:n.566T>C
|
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