ENST00000262493.12:c.1016T>A
MANE Select
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ENSP00000262493.6:p.Val339Asp
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ENST00000562316.6:c.545-1099T>A
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ENSP00000457238.2:n.545-1099T>A
|
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ENST00000564727.2:c.303+17T>A
|
ENSP00000454971.2:n.303+17T>A
|
|
ENST00000568375.2:c.254T>A
|
|
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ENST00000638210.1:n.1316T>A
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|
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ENST00000638705.1:c.1016T>A
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ENSP00000491223.1:p.Val339Asp
|
|
ENST00000638836.1:n.926T>A
|
|
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ENST00000639251.1:n.917T>A
|
|
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ENST00000639268.1:c.651T>A
|
|
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ENST00000639341.1:c.541T>A
|
|
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ENST00000639770.1:c.1054T>A
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ENSP00000491999.1:n.1054T>A
|
|
ENST00000640390.1:n.946T>A
|
|
|
ENST00000640469.1:c.380T>A
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ENSP00000491875.1:p.Val127Asp
|
|
ENST00000640560.1:n.792T>A
|
|
|
ENST00000640893.1:c.*414T>A
|
ENSP00000492677.1:n.*414T>A
|
|
ENST00000262493.10:c.1016T>A
|
ENSP00000262493.6:p.Val339Asp
|
|
ENST00000564727.1:c.236T>A
|
ENSP00000454971.1:p.Val79Asp
|
|
ENST00000568375.1:n.254T>A
|
|
|
NM_020988.2:c.1016T>A
|
NP_066268.1:p.Val339Asp
|
|
XM_011523003.1:c.890T>A
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XP_011521305.1:p.Val297Asp
|
|
XM_011523003.3:c.890T>A
|
XP_011521305.1:p.Val297Asp
|
|
NM_020988.3:c.1016T>A
MANE Select
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NP_066268.1:p.Val339Asp
|
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