ENST00000304874.14:c.922G>T
MANE Select
|
ENSP00000307188.9:p.Ala308Ser
|
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ENST00000362000.10:c.727G>T
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ENSP00000354710.6:p.Ala243Ser
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ENST00000380839.9:c.844G>T
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ENSP00000370219.4:p.Ala282Ser
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ENST00000395331.4:c.918+104G>T
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ENSP00000378740.3:n.918+104G>T
|
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ENST00000395332.8:c.922G>T
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ENSP00000378741.3:p.Ala308Ser
|
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ENST00000488343.2:c.91G>T
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ENSP00000500864.1:p.Ala31Ser
|
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ENST00000671817.1:c.844G>T
|
ENSP00000500462.1:p.Ala282Ser
|
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ENST00000672498.1:c.*221G>T
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ENSP00000500227.1:n.*221G>T
|
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ENST00000672586.1:n.1681G>T
|
|
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ENST00000672676.1:n.1946G>T
|
|
|
ENST00000673149.1:n.734G>T
|
|
|
ENST00000673350.1:n.3039G>T
|
|
|
ENST00000673518.1:c.844G>T
|
ENSP00000499889.1:p.Ala282Ser
|
|
ENST00000304874.13:c.922G>T
|
ENSP00000307188.9:p.Ala308Ser
|
|
ENST00000380839.8:c.844G>T
|
ENSP00000370219.4:p.Ala282Ser
|
|
ENST00000395331.3:c.918+104G>T
|
ENSP00000378740.3:n.918+104G>T
|
|
ENST00000395332.7:c.922G>T
|
ENSP00000378741.3:p.Ala308Ser
|
|
ENST00000450043.2:c.235G>T
|
ENSP00000396527.2:p.Ala79Ser
|
|
ENST00000464970.1:n.41G>T
|
|
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ENST00000488343.1:n.91G>T
|
|
|
ENST00000493708.5:n.403G>T
|
|
|
NM_000048.3:c.922G>T
|
NP_000039.2:p.Ala308Ser
|
|
NM_001024943.1:c.922G>T
|
NP_001020114.1:p.Ala308Ser
|
|
NM_001024944.1:c.918+104G>T
|
NP_001020115.1:n.918+104G>T
|
|
NM_001024946.1:c.844G>T
|
NP_001020117.1:p.Ala282Ser
|
|
NM_000048.4:c.922G>T
MANE Select
|
NP_000039.2:p.Ala308Ser
|
|
NM_001024943.2:c.922G>T
|
NP_001020114.1:p.Ala308Ser
|
|
NM_001024944.2:c.918+104G>T
|
NP_001020115.1:n.918+104G>T
|
|
NM_001024946.2:c.844G>T
|
NP_001020117.1:p.Ala282Ser
|
|