ENST00000375190.10:c.1022G>A
MANE Select
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ENSP00000364336.4:p.Gly341Glu
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ENST00000375190.8:c.1022G>A
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ENSP00000364336.3:p.Gly341Glu
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ENST00000411851.3:c.983+39G>A
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ENSP00000393333.2:n.983+39G>A
|
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ENST00000589966.1:c.633G>A
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ENSP00000468145.1:p.Arg211=
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NM_001060.5:c.1022G>A , LRG_578t1:c.1022G>A
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NP_001051.1:p.Gly341Glu
|
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NM_201636.2:c.983+39G>A
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NP_963998.2:n.983+39G>A
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XM_011528214.1:c.1022G>A
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XP_011526516.1:p.Gly341Glu
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XM_011528214.2:c.1022G>A
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XP_011526516.1:p.Gly341Glu
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NM_001060.6:c.1022G>A
MANE Select
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NP_001051.1:p.Gly341Glu
|
|
NM_201636.3:c.983+39G>A
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NP_963998.2:n.983+39G>A
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