ENST00000355832.10:c.3796A>G
MANE Select
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ENSP00000348089.5:p.Met1266Val
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ENST00000679552.1:n.867A>G
|
|
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ENST00000679871.1:n.942A>G
|
|
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ENST00000679974.1:n.845A>G
|
|
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ENST00000681632.1:n.5199A>G
|
|
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ENST00000681659.1:c.3637A>G
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ENSP00000505631.1:p.Met1213Val
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ENST00000355832.9:c.3796A>G
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ENSP00000348089.5:p.Met1266Val
|
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ENST00000465653.1:n.118A>G
|
|
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ENST00000623073.3:c.*2092A>G
|
ENSP00000485650.1:n.*2092A>G
|
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ENST00000623115.3:c.1906A>G
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ENSP00000485321.1:p.Met636Val
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ENST00000624341.3:c.1628A>G
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|
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NM_000124.3:c.3796A>G
|
NP_000115.1:p.Met1266Val
|
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XR_945953.1:n.243-10026T>C
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|
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NM_001346440.1:c.3796A>G
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NP_001333369.1:p.Met1266Val
|
|
NM_000124.4:c.3796A>G
MANE Select
|
NP_000115.1:p.Met1266Val
|
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NM_001346440.2:c.3796A>G
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NP_001333369.1:p.Met1266Val
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