ENST00000394867.9:n.1278G=
|
|
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ENST00000687128.1:n.1278G=
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|
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ENST00000688002.1:n.1133G=
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|
|
ENST00000689792.1:n.743G=
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|
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ENST00000262948.10:c.839G=
MANE Select
|
ENSP00000262948.4:p.Gly280=
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ENST00000262948.9:c.839G=
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ENSP00000262948.3:p.Gly280=
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|
ENST00000394867.8:c.548G=
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ENSP00000378336.1:p.Gly183=
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ENST00000593364.5:n.786G=
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|
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ENST00000595715.1:n.654G=
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|
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ENST00000597263.5:n.169+1738G=
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ENST00000599021.1:c.29+1738G=
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ENST00000600584.5:n.1399G=
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|
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ENST00000601786.5:n.1140G=
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|
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NM_030662.3:c.839G= , LRG_750t1:c.839G=
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NP_109587.1:p.Gly280=
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|
XM_006722799.2:c.705+1738G=
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XP_006722862.1:n.705+1738G=
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|
XM_011528133.1:c.269G=
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XP_011526435.1:p.Gly90=
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|
XM_017026989.1:c.839G=
|
XP_016882478.1:p.Gly280=
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|
XM_017026990.1:c.705+1738G=
|
XP_016882479.1:n.705+1738G=
|
|
NM_030662.4:c.839G=
MANE Select
|
NP_109587.1:p.Gly280=
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