ENST00000695651.1:n.1091G>T
|
|
|
ENST00000695652.1:c.2620G>T
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ENSP00000512083.1:p.Ala874Ser
|
|
ENST00000695653.1:c.652G>T
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ENSP00000512084.1:p.Ala218Ser
|
|
ENST00000695654.1:c.1867G>T
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ENSP00000512085.1:p.Ala623Ser
|
|
ENST00000695655.1:c.1684G>T
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ENSP00000512086.1:n.1684G>T
|
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ENST00000695692.1:n.2107G>T
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|
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ENST00000245907.11:c.2743G>T
MANE Select
|
ENSP00000245907.4:p.Ala915Ser
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ENST00000245907.10:c.2743G>T
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ENSP00000245907.4:p.Ala915Ser
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|
ENST00000594005.1:n.319G>T
|
|
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NM_000064.3:c.2743G>T
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NP_000055.2:p.Ala915Ser
|
|
NM_000064.4:c.2743G>T
MANE Select
|
NP_000055.2:p.Ala915Ser
|
|