ENST00000270357.10:c.1558G>T
MANE Select
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ENSP00000270357.4:p.Glu520Ter
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ENST00000270357.8:c.865G>T
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ENSP00000270357.3:p.Glu289Ter
|
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ENST00000437406.1:c.124G>T
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ENSP00000403319.1:p.Glu42Ter
|
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ENST00000451363.5:c.199G>T
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ENSP00000414661.1:p.Glu67Ter
|
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ENST00000464550.5:n.394G>T
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|
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ENST00000471657.1:n.361G>T
|
|
|
ENST00000481757.5:n.2492G>T
|
|
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ENST00000486058.5:n.1671G>T
|
|
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ENST00000493398.5:n.704G>T
|
|
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NM_018226.4:c.1558G>T
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NP_060696.4:p.Glu520Ter
|
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XM_005247036.3:c.1525G>T
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XP_005247093.1:p.Glu509Ter
|
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NM_018226.5:c.1558G>T
|
NP_060696.4:p.Glu520Ter
|
|
XM_005247036.4:c.1525G>T
|
XP_005247093.1:p.Glu509Ter
|
|
NM_018226.6:c.1558G>T
MANE Select
|
NP_060696.4:p.Glu520Ter
|
|