ENST00000340855.11:c.1159G>C
MANE Select
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ENSP00000339801.6:p.Ala387Pro
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ENST00000651111.1:c.526G>C
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ENSP00000498395.1:p.Ala176Pro
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ENST00000340855.10:c.1159G>C
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ENSP00000339801.6:p.Ala387Pro
|
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ENST00000422081.6:c.526G>C
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ENSP00000477056.1:p.Ala176Pro
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ENST00000441880.1:n.266G>C
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|
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NM_000202.6:c.1159G>C
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NP_000193.1:p.Ala387Pro
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NM_001166550.2:c.889G>C
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NP_001160022.1:p.Ala297Pro
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NM_000202.7:c.1159G>C
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NP_000193.1:p.Ala387Pro
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NM_001166550.3:c.889G>C
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NP_001160022.1:p.Ala297Pro
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NM_000202.8:c.1159G>C
MANE Select
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NP_000193.1:p.Ala387Pro
|
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NM_001166550.4:c.889G>C
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NP_001160022.1:p.Ala297Pro
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