ENST00000233190.11:c.1790T>G
MANE Select
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ENSP00000233190.5:p.Val597Gly
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ENST00000233190.10:c.1790T>G
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ENSP00000233190.5:p.Val597Gly
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ENST00000423725.5:c.1619T>G
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ENSP00000397760.1:p.Val540Gly
|
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ENST00000432169.5:c.1457T>G
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ENSP00000409689.1:p.Val486Gly
|
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ENST00000440274.5:c.1682T>G
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ENSP00000409766.1:p.Val561Gly
|
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ENST00000449699.5:c.1790T>G
|
ENSP00000399912.1:p.Val597Gly
|
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ENST00000455934.6:c.1832T>G
|
ENSP00000392709.2:p.Val611Gly
|
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ENST00000457011.5:c.1442T>G
|
ENSP00000400976.1:p.Val481Gly
|
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ENST00000498520.1:n.262T>G
|
|
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NM_001199981.1:c.1682T>G
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NP_001186910.1:p.Val561Gly
|
|
NM_001199982.1:c.1457T>G
|
NP_001186911.1:p.Val486Gly
|
|
NM_001199983.1:c.1619T>G
|
NP_001186912.1:p.Val540Gly
|
|
NM_001199984.1:c.1832T>G
|
NP_001186913.1:p.Val611Gly
|
|
NM_005006.6:c.1790T>G
|
NP_004997.4:p.Val597Gly
|
|
XM_017004188.2:c.1031T>G
|
XP_016859677.1:p.Val344Gly
|
|
NM_001199981.2:c.1682T>G
|
NP_001186910.1:p.Val561Gly
|
|
NM_001199982.2:c.1457T>G
|
NP_001186911.1:p.Val486Gly
|
|
NM_001199983.2:c.1619T>G
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NP_001186912.1:p.Val540Gly
|
|
NM_005006.7:c.1790T>G
MANE Select
|
NP_004997.4:p.Val597Gly
|
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NM_001199984.2:c.1832T>G
|
NP_001186913.1:p.Val611Gly
|
|