ENST00000233190.11:c.854G>A
MANE Select
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ENSP00000233190.5:p.Trp285Ter
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ENST00000233190.10:c.854G>A
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ENSP00000233190.5:p.Trp285Ter
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|
ENST00000423725.5:c.683G>A
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ENSP00000397760.1:p.Trp228Ter
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ENST00000432169.5:c.521G>A
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ENSP00000409689.1:p.Trp174Ter
|
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ENST00000440274.5:c.746G>A
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ENSP00000409766.1:p.Trp249Ter
|
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ENST00000449699.5:c.854G>A
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ENSP00000399912.1:p.Trp285Ter
|
|
ENST00000455934.6:c.896G>A
|
ENSP00000392709.2:p.Trp299Ter
|
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ENST00000457011.5:c.506G>A
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ENSP00000400976.1:p.Trp169Ter
|
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NM_001199981.1:c.746G>A
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NP_001186910.1:p.Trp249Ter
|
|
NM_001199982.1:c.521G>A
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NP_001186911.1:p.Trp174Ter
|
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NM_001199983.1:c.683G>A
|
NP_001186912.1:p.Trp228Ter
|
|
NM_001199984.1:c.896G>A
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NP_001186913.1:p.Trp299Ter
|
|
NM_005006.6:c.854G>A
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NP_004997.4:p.Trp285Ter
|
|
XM_017004188.2:c.95G>A
|
XP_016859677.1:p.Trp32Ter
|
|
NM_001199981.2:c.746G>A
|
NP_001186910.1:p.Trp249Ter
|
|
NM_001199982.2:c.521G>A
|
NP_001186911.1:p.Trp174Ter
|
|
NM_001199983.2:c.683G>A
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NP_001186912.1:p.Trp228Ter
|
|
NM_005006.7:c.854G>A
MANE Select
|
NP_004997.4:p.Trp285Ter
|
|
NM_001199984.2:c.896G>A
|
NP_001186913.1:p.Trp299Ter
|
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