ENST00000695666.1:n.865T>G
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|
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ENST00000695667.1:n.383T>G
|
|
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ENST00000695668.1:n.2363T>G
|
|
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ENST00000300692.9:c.378T>G
MANE Select
|
ENSP00000300692.4:p.Ala126=
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ENST00000300692.8:c.378T>G
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ENSP00000300692.4:p.Ala126=
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ENST00000392884.2:c.275-309T>G
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ENSP00000376622.2:n.275-309T>G
|
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ENST00000526561.1:n.80-309T>G
|
|
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ENST00000529594.5:c.159T>G
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ENSP00000437335.1:p.Ala53=
|
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ENST00000534687.5:c.288-309T>G
|
|
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NM_000732.4:c.378T>G , LRG_37t1:c.378T>G
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NP_000723.1:p.Ala126=
|
|
NM_001040651.1:c.275-309T>G
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NP_001035741.1:n.275-309T>G
|
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NM_001040651.2:c.275-309T>G
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NP_001035741.1:n.275-309T>G
|
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NM_000732.6:c.378T>G
MANE Select
|
NP_000723.1:p.Ala126=
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|