ENST00000233190.11:c.788T>G
MANE Select
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ENSP00000233190.5:p.Val263Gly
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ENST00000233190.10:c.788T>G
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ENSP00000233190.5:p.Val263Gly
|
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ENST00000423725.5:c.617T>G
|
ENSP00000397760.1:p.Val206Gly
|
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ENST00000432169.5:c.455T>G
|
ENSP00000409689.1:p.Val152Gly
|
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ENST00000440274.5:c.680T>G
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ENSP00000409766.1:p.Val227Gly
|
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ENST00000449699.5:c.788T>G
|
ENSP00000399912.1:p.Val263Gly
|
|
ENST00000455934.6:c.830T>G
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ENSP00000392709.2:p.Val277Gly
|
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ENST00000457011.5:c.440T>G
|
ENSP00000400976.1:p.Val147Gly
|
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NM_001199981.1:c.680T>G
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NP_001186910.1:p.Val227Gly
|
|
NM_001199982.1:c.455T>G
|
NP_001186911.1:p.Val152Gly
|
|
NM_001199983.1:c.617T>G
|
NP_001186912.1:p.Val206Gly
|
|
NM_001199984.1:c.830T>G
|
NP_001186913.1:p.Val277Gly
|
|
NM_005006.6:c.788T>G
|
NP_004997.4:p.Val263Gly
|
|
XM_017004188.2:c.29T>G
|
XP_016859677.1:p.Val10Gly
|
|
NM_001199981.2:c.680T>G
|
NP_001186910.1:p.Val227Gly
|
|
NM_001199982.2:c.455T>G
|
NP_001186911.1:p.Val152Gly
|
|
NM_001199983.2:c.617T>G
|
NP_001186912.1:p.Val206Gly
|
|
NM_005006.7:c.788T>G
MANE Select
|
NP_004997.4:p.Val263Gly
|
|
NM_001199984.2:c.830T>G
|
NP_001186913.1:p.Val277Gly
|
|