ENST00000452035.7:n.2330T>G
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ENST00000483004.2:c.1627T>G
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ENSP00000419887.2:p.Cys543Gly
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ENST00000698628.1:c.1625-212T>G
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ENSP00000513848.1:n.1625-212T>G
|
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ENST00000698629.1:n.2115T>G
|
|
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ENST00000698630.1:n.2559T>G
|
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ENST00000698631.1:n.2560T>G
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|
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ENST00000698632.1:n.3449T>G
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|
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ENST00000698633.1:n.3339T>G
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|
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ENST00000425368.7:c.1843T>G
MANE Select
|
ENSP00000416561.2:p.Cys615Gly
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ENST00000425368.6:c.1843T>G
|
ENSP00000416561.2:p.Cys615Gly
|
|
ENST00000456570.5:c.3349T>G
|
ENSP00000410815.1:p.Cys1117Gly
|
|
ENST00000467360.1:n.969T>G
|
|
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ENST00000477310.1:c.2896T>G
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ENSP00000418996.1:p.Cys966Gly
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ENST00000482312.1:n.59T>G
|
|
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ENST00000483004.1:c.465T>G
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|
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NM_001710.5:c.1843T>G , LRG_136t1:c.1843T>G
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NP_001701.2:p.Cys615Gly
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|
NM_001710.6:c.1843T>G
MANE Select
|
NP_001701.2:p.Cys615Gly
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