ENST00000355112.8:c.2993T>C
MANE Select
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ENSP00000347232.3:p.Val998Ala
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ENST00000560559.2:n.1566T>C
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|
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ENST00000648453.1:c.2993T>C
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ENSP00000497646.1:p.Val998Ala
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ENST00000680772.1:c.2993T>C
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ENSP00000506117.1:p.Val998Ala
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ENST00000681142.1:c.2993T>C
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ENSP00000506682.1:p.Val998Ala
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ENST00000355112.7:c.2993T>C
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ENSP00000347232.3:p.Val998Ala
|
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ENST00000559724.5:c.*1917T>C
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ENSP00000453359.1:n.*1917T>C
|
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ENST00000560136.5:n.1019T>C
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|
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ENST00000560509.5:c.2993T>C
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ENSP00000454158.1:p.Val998Ala
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ENST00000560559.1:n.530T>C
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|
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NM_000057.3:c.2993T>C
|
NP_000048.1:p.Val998Ala
|
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NM_001287246.1:c.2993T>C
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NP_001274175.1:p.Val998Ala
|
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NM_001287247.1:c.2993T>C
|
NP_001274176.1:p.Val998Ala
|
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NM_001287248.1:c.1868T>C
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NP_001274177.1:p.Val623Ala
|
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XM_006720632.2:c.1031T>C
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XP_006720695.1:p.Val344Ala
|
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XM_011521881.1:c.1679T>C
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XP_011520183.1:p.Val560Ala
|
|
XM_011521881.2:c.1679T>C
|
XP_011520183.1:p.Val560Ala
|
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NM_000057.4:c.2993T>C
MANE Select
|
NP_000048.1:p.Val998Ala
|
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NM_001287246.2:c.2993T>C
|
NP_001274175.1:p.Val998Ala
|
|
NM_001287247.2:c.2993T>C
|
NP_001274176.1:p.Val998Ala
|
|
NM_001287248.2:c.1868T>C
|
NP_001274177.1:p.Val623Ala
|
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