ENST00000233190.11:c.802G>A
MANE Select
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ENSP00000233190.5:p.Gly268Arg
|
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ENST00000233190.10:c.802G>A
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ENSP00000233190.5:p.Gly268Arg
|
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ENST00000423725.5:c.631G>A
|
ENSP00000397760.1:p.Gly211Arg
|
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ENST00000432169.5:c.469G>A
|
ENSP00000409689.1:p.Gly157Arg
|
|
ENST00000440274.5:c.694G>A
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ENSP00000409766.1:p.Gly232Arg
|
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ENST00000449699.5:c.802G>A
|
ENSP00000399912.1:p.Gly268Arg
|
|
ENST00000455934.6:c.844G>A
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ENSP00000392709.2:p.Gly282Arg
|
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ENST00000457011.5:c.454G>A
|
ENSP00000400976.1:p.Gly152Arg
|
|
NM_001199981.1:c.694G>A
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NP_001186910.1:p.Gly232Arg
|
|
NM_001199982.1:c.469G>A
|
NP_001186911.1:p.Gly157Arg
|
|
NM_001199983.1:c.631G>A
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NP_001186912.1:p.Gly211Arg
|
|
NM_001199984.1:c.844G>A
|
NP_001186913.1:p.Gly282Arg
|
|
NM_005006.6:c.802G>A
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NP_004997.4:p.Gly268Arg
|
|
XM_017004188.2:c.43G>A
|
XP_016859677.1:p.Gly15Arg
|
|
NM_001199981.2:c.694G>A
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NP_001186910.1:p.Gly232Arg
|
|
NM_001199982.2:c.469G>A
|
NP_001186911.1:p.Gly157Arg
|
|
NM_001199983.2:c.631G>A
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NP_001186912.1:p.Gly211Arg
|
|
NM_005006.7:c.802G>A
MANE Select
|
NP_004997.4:p.Gly268Arg
|
|
NM_001199984.2:c.844G>A
|
NP_001186913.1:p.Gly282Arg
|
|