NM_014797.3:c.1222T>G
MANE Select
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NP_055612.2:p.Cys408Gly
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ENST00000230122.4:c.1222T>G
MANE Select
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ENSP00000230122.4:p.Cys408Gly
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NM_014797.2:c.1222T>G , LRG_326t1:c.1222T>G
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NP_055612.2:p.Cys408Gly
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ENST00000230122.3:c.1222T>G
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ENSP00000230122.3:p.Cys408Gly
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ENST00000698513.1:c.1054T>G
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ENSP00000513763.1:p.Cys352Gly
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ENST00000698514.1:c.*80T>G
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ENSP00000513764.1:n.*80T>G
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ENST00000698515.1:c.*80T>G
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ENSP00000513765.1:n.*80T>G
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ENST00000698516.1:c.1222T>G
|
ENSP00000513766.1:p.Cys408Gly
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ENST00000698517.1:n.2062T>G
|
|
ENST00000698518.1:c.1222T>G
|
ENSP00000513767.1:p.Cys408Gly
|
ENST00000698519.1:c.1054T>G
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ENSP00000513768.1:p.Cys352Gly
|
ENST00000698520.1:c.952+5610T>G
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ENSP00000513769.1:n.952+5610T>G
|