NM_000170.3:c.2281G=
MANE Select
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NP_000161.2:p.Gly761=
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ENST00000321612.8:c.2281G=
MANE Select
|
ENSP00000370737.4:p.Gly761=
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NM_000170.2:c.2281G= , LRG_643t1:c.2281G=
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NP_000161.2:p.Gly761=
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ENST00000321612.6:c.2281G=
|
ENSP00000370737.3:p.Gly761=
|
ENST00000467946.1:n.207G=
|
|
ENST00000638233.1:n.716G=
|
|
ENST00000638661.1:c.481G=
|
ENSP00000491369.1:p.Gly161=
|
ENST00000638694.1:n.468G=
|
|
ENST00000639318.1:c.481G=
|
ENSP00000491932.1:p.Gly161=
|
ENST00000639364.1:n.1981G=
|
|
ENST00000639443.1:n.1849G=
|
|
ENST00000639639.1:c.-18G=
|
ENSP00000491312.1:n.-18G=
|
ENST00000639954.1:n.1989G=
|
|
ENST00000640505.1:n.520G=
|
|