ENST00000356487.11:c.1499T>C
MANE Select
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ENSP00000348877.3:p.Val500Ala
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ENST00000415930.8:c.1616T>C
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ENSP00000405573.3:p.Val539Ala
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ENST00000586425.2:c.1165T>C
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ENST00000588991.7:c.1532T>C
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ENSP00000465858.3:p.Val511Ala
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ENST00000643067.1:n.2544T>C
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ENST00000647446.1:c.*550T>C
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ENSP00000495129.1:n.*550T>C
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ENST00000356487.9:c.1499T>C
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ENSP00000348877.3:p.Val500Ala
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ENST00000415930.7:c.1532T>C
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ENSP00000405573.2:p.Val511Ala
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ENST00000586077.1:n.2461T>C
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ENST00000586392.1:n.1237T>C
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ENST00000586425.1:c.1399-158T>C
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ENSP00000467670.2:n.1399-158T>C
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ENST00000588991.6:c.1544T>C
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ENSP00000465858.2:p.Val515Ala
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ENST00000592740.5:c.193+3086T>C
|
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NM_000175.3:c.1499T>C
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NP_000166.2:p.Val500Ala
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NM_001184722.1:c.1532T>C
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NP_001171651.1:p.Val511Ala
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NM_001289789.1:c.1616T>C
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NP_001276718.1:p.Val539Ala
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NM_001289790.1:c.1415T>C
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NP_001276719.1:p.Val472Ala
|
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XM_005258764.1:c.1499T>C
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XP_005258821.1:p.Val500Ala
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XM_006723148.1:c.1499T>C
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XP_006723211.1:p.Val500Ala
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XM_011526754.1:c.1616T>C
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XP_011525056.1:p.Val539Ala
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NM_000175.5:c.1499T>C
MANE Select
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NP_000166.2:p.Val500Ala
|
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NM_001289790.2:c.1415T>C
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NP_001276719.1:p.Val472Ala
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NM_001329909.1:c.1499T>C
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NP_001316838.1:p.Val500Ala
|
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NM_001329910.1:c.1499T>C
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NP_001316839.1:p.Val500Ala
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NM_001329911.1:c.1472T>C
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NP_001316840.1:p.Val491Ala
|
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XM_011526754.3:c.1616T>C
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XP_011525056.1:p.Val539Ala
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NM_001289790.3:c.1415T>C
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NP_001276719.1:p.Val472Ala
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NM_001329911.2:c.1472T>C
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NP_001316840.1:p.Val491Ala
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