ENST00000340855.11:c.1133T>G
MANE Select
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ENSP00000339801.6:p.Phe378Cys
|
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ENST00000651111.1:c.500T>G
|
ENSP00000498395.1:p.Phe167Cys
|
|
ENST00000340855.10:c.1133T>G
|
ENSP00000339801.6:p.Phe378Cys
|
|
ENST00000422081.6:c.500T>G
|
ENSP00000477056.1:p.Phe167Cys
|
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ENST00000441880.1:n.240T>G
|
|
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NM_000202.6:c.1133T>G
|
NP_000193.1:p.Phe378Cys
|
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NM_001166550.2:c.863T>G
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NP_001160022.1:p.Phe288Cys
|
|
NM_000202.7:c.1133T>G
|
NP_000193.1:p.Phe378Cys
|
|
NM_001166550.3:c.863T>G
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NP_001160022.1:p.Phe288Cys
|
|
NM_000202.8:c.1133T>G
MANE Select
|
NP_000193.1:p.Phe378Cys
|
|
NM_001166550.4:c.863T>G
|
NP_001160022.1:p.Phe288Cys
|
|