ENST00000372470.9:c.389T>C
MANE Select
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ENSP00000361548.3:p.Val130Ala
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ENST00000413998.7:c.368T>C
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ENSP00000414004.3:p.Val123Ala
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ENST00000638732.1:n.389T>C
|
|
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ENST00000372470.7:c.389T>C
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ENSP00000361548.3:p.Val130Ala
|
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ENST00000413998.6:c.389T>C
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ENSP00000414004.2:p.Val130Ala
|
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ENST00000612993.1:c.389T>C
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ENSP00000480273.1:p.Val130Ala
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NM_005373.2:c.389T>C , LRG_510t1:c.389T>C
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NP_005364.1:p.Val130Ala
|
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XM_011541478.1:c.368T>C
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XP_011539780.1:p.Val123Ala
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XM_017001320.1:c.560T>C
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XP_016856809.1:p.Val187Ala
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NM_005373.3:c.389T>C
MANE Select
|
NP_005364.1:p.Val130Ala
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|