ENST00000383788.10:c.1076T>A
MANE Select
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ENSP00000373298.3:p.Leu359Gln
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ENST00000604401.2:n.932T>A
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|
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ENST00000679838.1:c.*838T>A
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ENSP00000505708.1:n.*838T>A
|
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ENST00000680240.1:n.988T>A
|
|
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ENST00000680545.1:n.842T>A
|
|
|
ENST00000681097.1:c.*90T>A
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ENSP00000505397.1:n.*90T>A
|
|
ENST00000681222.1:n.4567T>A
|
|
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ENST00000383781.8:c.1046T>A
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ENSP00000373291.3:p.Leu349Gln
|
|
ENST00000383786.9:c.974T>A
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ENSP00000373296.3:p.Leu325Gln
|
|
ENST00000383788.9:c.1076T>A
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ENSP00000373298.3:p.Leu359Gln
|
|
ENST00000603808.5:c.1076T>A
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ENSP00000474271.1:p.Leu359Gln
|
|
NM_005677.3:c.1076T>A
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NP_005668.2:p.Leu359Gln
|
|
NM_080538.2:c.1046T>A
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NP_536799.1:p.Leu349Gln
|
|
NM_080539.3:c.974T>A
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NP_536800.2:p.Leu325Gln
|
|
NM_005677.4:c.1076T>A
MANE Select
|
NP_005668.2:p.Leu359Gln
|
|
NM_080539.4:c.974T>A
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NP_536800.2:p.Leu325Gln
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