ENST00000322213.9:c.3333C>G
MANE Select
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ENSP00000323421.3:p.Ile1111Met
|
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ENST00000674590.1:c.2565C>G
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ENSP00000502626.1:p.Ile855Met
|
|
ENST00000675504.1:c.3267C>G
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ENSP00000502524.1:p.Ile1089Met
|
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ENST00000322213.8:c.3333C>G
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ENSP00000323421.3:p.Ile1111Met
|
|
ENST00000375340.10:c.3267C>G
|
ENSP00000364489.7:p.Ile1089Met
|
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ENST00000469129.1:n.189C>G
|
|
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ENST00000470241.2:c.623C>G
|
|
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NM_001281463.1:c.3267C>G , LRG_773t1:c.3267C>G
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NP_001268392.1:p.Ile1089Met
|
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NM_006306.3:c.3333C>G , LRG_773t2:c.3333C>G
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NP_006297.2:p.Ile1111Met
|
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NM_006306.4:c.3333C>G
MANE Select
|
NP_006297.2:p.Ile1111Met
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