ENST00000233190.11:c.837G>A
MANE Select
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ENSP00000233190.5:p.Glu279=
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ENST00000233190.10:c.837G>A
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ENSP00000233190.5:p.Glu279=
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|
ENST00000423725.5:c.666G>A
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ENSP00000397760.1:p.Glu222=
|
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ENST00000432169.5:c.504G>A
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ENSP00000409689.1:p.Glu168=
|
|
ENST00000440274.5:c.729G>A
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ENSP00000409766.1:p.Glu243=
|
|
ENST00000449699.5:c.837G>A
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ENSP00000399912.1:p.Glu279=
|
|
ENST00000455934.6:c.879G>A
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ENSP00000392709.2:p.Glu293=
|
|
ENST00000457011.5:c.489G>A
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ENSP00000400976.1:p.Glu163=
|
|
NM_001199981.1:c.729G>A
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NP_001186910.1:p.Glu243=
|
|
NM_001199982.1:c.504G>A
|
NP_001186911.1:p.Glu168=
|
|
NM_001199983.1:c.666G>A
|
NP_001186912.1:p.Glu222=
|
|
NM_001199984.1:c.879G>A
|
NP_001186913.1:p.Glu293=
|
|
NM_005006.6:c.837G>A
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NP_004997.4:p.Glu279=
|
|
XM_017004188.2:c.78G>A
|
XP_016859677.1:p.Glu26=
|
|
NM_001199981.2:c.729G>A
|
NP_001186910.1:p.Glu243=
|
|
NM_001199982.2:c.504G>A
|
NP_001186911.1:p.Glu168=
|
|
NM_001199983.2:c.666G>A
|
NP_001186912.1:p.Glu222=
|
|
NM_005006.7:c.837G>A
MANE Select
|
NP_004997.4:p.Glu279=
|
|
NM_001199984.2:c.879G>A
|
NP_001186913.1:p.Glu293=
|
|