ENST00000445590.4:c.438A>C
MANE Select
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ENSP00000414451.2:p.Gly146=
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ENST00000360827.6:c.438A>C
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ENSP00000354070.2:p.Gly146=
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ENST00000391880.6:c.*579A>C
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ENSP00000375752.2:n.*579A>C
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ENST00000445590.3:c.438A>C
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ENSP00000414451.2:p.Gly146=
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NM_207468.2:c.438A>C
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NP_997351.2:p.Gly146=
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XM_006711318.2:c.241+2938A>C
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XP_006711381.1:n.241+2938A>C
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NM_001324080.1:c.438A>C
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NP_001311009.1:p.Gly146=
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NR_136691.1:n.1208A>C
|
|
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XM_017001279.1:c.438A>C
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XP_016856768.1:p.Gly146=
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XM_017001280.1:c.438A>C
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XP_016856769.1:p.Gly146=
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|
XM_017001281.1:c.438A>C
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XP_016856770.1:p.Gly146=
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|
XM_017001282.1:c.438A>C
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XP_016856771.1:p.Gly146=
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XM_017001285.1:c.274+2938A>C
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XP_016856774.1:n.274+2938A>C
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NM_001324080.2:c.438A>C
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NP_001311009.1:p.Gly146=
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|
NM_207468.3:c.438A>C
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NP_997351.2:p.Gly146=
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NR_136691.2:n.1222A>C
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|
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NM_001394345.1:c.438A>C
MANE Select
|
NP_001381274.1:p.Gly146=
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