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NM_001386809.1:c.542C>T
MANE Select
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NP_001373738.1:p.Ala181Val
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ENST00000293778.12:c.542C>T
MANE Select
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ENSP00000293778.7:p.Ala181Val
|
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NM_001100812.1:c.599C>T
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NP_001094282.1:p.Ala200Val
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NM_001100812.2:c.542C>T
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NP_001094282.2:p.Ala181Val
|
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NM_022059.3:c.599C>T
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NP_071342.2:p.Ala200Val
|
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NM_022059.4:c.599C>T
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NP_071342.2:p.Ala200Val
|
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ENST00000293778.10:c.599C>T
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ENSP00000293778.6:p.Ala200Val
|
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ENST00000574412.5:c.599C>T
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ENSP00000459592.1:p.Ala200Val
|
|
ENST00000574412.6:c.542C>T
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ENSP00000459592.2:p.Ala181Val
|
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ENST00000575168.1:n.373C>T
|
|
|
ENST00000576153.5:n.333C>T
|
|