ENST00000330377.3:c.436A>G
MANE Select
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ENSP00000329312.2:p.Thr146Ala
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ENST00000249053.3:c.*65A>G
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ENSP00000249053.3:n.*65A>G
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ENST00000330377.2:c.436A>G
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ENSP00000329312.2:p.Thr146Ala
|
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ENST00000438703.1:c.439A>G
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ENSP00000403391.1:p.Thr147Ala
|
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NM_020070.3:c.436A>G
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NP_064455.1:p.Thr146Ala
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NM_152855.2:c.*65A>G
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NP_690594.1:n.*65A>G
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XM_011530169.1:c.439A>G
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XP_011528471.1:p.Thr147Ala
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XM_011530169.2:c.439A>G
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XP_011528471.1:p.Thr147Ala
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NM_020070.4:c.436A>G
MANE Select
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NP_064455.1:p.Thr146Ala
|
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NM_001369906.1:c.439A>G
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NP_001356835.1:p.Thr147Ala
|
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NM_152855.3:c.*65A>G
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NP_690594.1:n.*65A>G
|
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