ENST00000695651.1:n.2645G>C
|
|
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ENST00000695653.1:c.2206G>C
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ENSP00000512084.1:p.Glu736Gln
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|
ENST00000695654.1:c.3322G>C
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ENSP00000512085.1:p.Glu1108Gln
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|
ENST00000695689.1:c.268G>C
|
ENSP00000512101.1:n.268G>C
|
|
ENST00000695690.1:n.488G>C
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|
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ENST00000695691.1:n.488G>C
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|
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ENST00000245907.11:c.4297G>C
MANE Select
|
ENSP00000245907.4:p.Glu1433Gln
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|
ENST00000245907.10:c.4297G>C
|
ENSP00000245907.4:p.Glu1433Gln
|
|
ENST00000596548.1:c.418G>C
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ENSP00000469744.1:p.Glu140Gln
|
|
ENST00000599899.5:n.1256G>C
|
|
|
ENST00000601008.1:c.242-4036G>C
|
ENSP00000471384.1:n.242-4036G>C
|
|
NM_000064.3:c.4297G>C
|
NP_000055.2:p.Glu1433Gln
|
|
NM_000064.4:c.4297G>C
MANE Select
|
NP_000055.2:p.Glu1433Gln
|
|