ENST00000330062.8:c.410G>T
MANE Select
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ENSP00000331897.4:p.Gly137Val
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ENST00000330062.7:c.410G>T
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ENSP00000331897.3:p.Gly137Val
|
|
ENST00000540499.2:c.254G>T
|
ENSP00000446147.2:p.Gly85Val
|
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ENST00000559482.5:c.208-209G>T
|
ENSP00000453016.1:n.208-209G>T
|
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ENST00000560061.1:c.*35G>T
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ENSP00000453254.1:n.*35G>T
|
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NM_001289910.1:c.254G>T , LRG_611t1:c.254G>T
|
NP_001276839.1:p.Gly85Val
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NM_001290114.1:c.20G>T
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NP_001277043.1:p.Gly7Val
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NM_002168.3:c.410G>T , LRG_611t2:c.410G>T
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NP_002159.2:p.Gly137Val
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NM_001290114.2:c.20G>T
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NP_001277043.1:p.Gly7Val
|
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NM_002168.4:c.410G>T
MANE Select
|
NP_002159.2:p.Gly137Val
|
|