ENST00000355832.10:c.3063T>G
MANE Select
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ENSP00000348089.5:p.Ile1021Met
|
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ENST00000679552.1:n.142-93T>G
|
|
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ENST00000679871.1:n.209T>G
|
|
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ENST00000679974.1:n.120-93T>G
|
|
|
ENST00000681632.1:n.4466T>G
|
|
|
ENST00000681659.1:c.2904T>G
|
ENSP00000505631.1:p.Ile968Met
|
|
ENST00000355832.9:c.3063T>G
|
ENSP00000348089.5:p.Ile1021Met
|
|
ENST00000623073.3:c.*1359T>G
|
ENSP00000485650.1:n.*1359T>G
|
|
ENST00000623115.3:c.1173T>G
|
ENSP00000485321.1:p.Ile391Met
|
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ENST00000624341.3:c.895T>G
|
|
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NM_000124.3:c.3063T>G
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NP_000115.1:p.Ile1021Met
|
|
XR_945953.1:n.243-583A>C
|
|
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NM_001346440.1:c.3063T>G
|
NP_001333369.1:p.Ile1021Met
|
|
NM_000124.4:c.3063T>G
MANE Select
|
NP_000115.1:p.Ile1021Met
|
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NM_001346440.2:c.3063T>G
|
NP_001333369.1:p.Ile1021Met
|
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