ENST00000233190.11:c.811A>G
MANE Select
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ENSP00000233190.5:p.Met271Val
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ENST00000233190.10:c.811A>G
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ENSP00000233190.5:p.Met271Val
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ENST00000423725.5:c.640A>G
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ENSP00000397760.1:p.Met214Val
|
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ENST00000432169.5:c.478A>G
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ENSP00000409689.1:p.Met160Val
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ENST00000440274.5:c.703A>G
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ENSP00000409766.1:p.Met235Val
|
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ENST00000449699.5:c.811A>G
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ENSP00000399912.1:p.Met271Val
|
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ENST00000455934.6:c.853A>G
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ENSP00000392709.2:p.Met285Val
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ENST00000457011.5:c.463A>G
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ENSP00000400976.1:p.Met155Val
|
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NM_001199981.1:c.703A>G
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NP_001186910.1:p.Met235Val
|
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NM_001199982.1:c.478A>G
|
NP_001186911.1:p.Met160Val
|
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NM_001199983.1:c.640A>G
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NP_001186912.1:p.Met214Val
|
|
NM_001199984.1:c.853A>G
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NP_001186913.1:p.Met285Val
|
|
NM_005006.6:c.811A>G
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NP_004997.4:p.Met271Val
|
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XM_017004188.2:c.52A>G
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XP_016859677.1:p.Met18Val
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NM_001199981.2:c.703A>G
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NP_001186910.1:p.Met235Val
|
|
NM_001199982.2:c.478A>G
|
NP_001186911.1:p.Met160Val
|
|
NM_001199983.2:c.640A>G
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NP_001186912.1:p.Met214Val
|
|
NM_005006.7:c.811A>G
MANE Select
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NP_004997.4:p.Met271Val
|
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NM_001199984.2:c.853A>G
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NP_001186913.1:p.Met285Val
|
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