ENST00000426263.10:c.1219G>T
MANE Select
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ENSP00000416293.2:p.Ala407Ser
|
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ENST00000674545.1:n.1836G>T
|
|
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ENST00000674765.1:c.1030-807G>T
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ENSP00000501811.1:n.1030-807G>T
|
|
ENST00000675112.1:n.1520G>T
|
|
|
ENST00000676254.1:n.1668G>T
|
|
|
ENST00000426263.7:c.1219G>T
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ENSP00000416293.2:p.Ala407Ser
|
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ENST00000475162.3:c.416-686G>T
|
|
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ENST00000630287.2:c.*534G>T
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ENSP00000486694.1:n.*534G>T
|
|
NM_006516.2:c.1219G>T
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NP_006507.2:p.Ala407Ser
|
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NM_006516.3:c.1219G>T
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NP_006507.2:p.Ala407Ser
|
|
NM_006516.4:c.1219G>T
MANE Select
|
NP_006507.2:p.Ala407Ser
|
|