ENST00000290866.10:c.2356G>T
MANE Select
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ENSP00000290866.4:p.Ala786Ser
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ENST00000290863.10:c.634G>T
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ENSP00000290863.6:p.Ala212Ser
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ENST00000290866.9:c.2356G>T
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ENSP00000290866.4:p.Ala786Ser
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ENST00000413513.7:c.634G>T
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ENSP00000392247.3:p.Ala212Ser
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ENST00000428043.5:c.2356G>T
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ENSP00000397593.2:p.Ala786Ser
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ENST00000577647.2:c.634G>T
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ENSP00000464149.1:p.Ala212Ser
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ENST00000578839.5:c.*426G>T
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ENSP00000462110.2:n.*426G>T
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ENST00000579204.1:c.615G>T
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ENSP00000464629.1:n.615G>T
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ENST00000579314.5:c.*85G>T
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ENSP00000462599.1:n.*85G>T
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ENST00000582005.5:c.*276G>T
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ENSP00000462002.1:n.*276G>T
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ENST00000582761.1:c.124G>T
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ENSP00000462909.1:p.Ala42Ser
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ENST00000584865.5:n.302G>T
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NM_000789.3:c.2356G>T
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NP_000780.1:p.Ala786Ser
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NM_001178057.1:c.634G>T
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NP_001171528.1:p.Ala212Ser
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NM_152830.2:c.634G>T
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NP_690043.1:p.Ala212Ser
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XM_005257110.1:c.1807G>T
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XP_005257167.1:p.Ala603Ser
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XM_006721737.2:c.694G>T
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XP_006721800.2:p.Ala232Ser
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XM_006721737.3:c.694G>T
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XP_006721800.2:p.Ala232Ser
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NM_000789.4:c.2356G>T
MANE Select
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NP_000780.1:p.Ala786Ser
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NM_001178057.2:c.634G>T
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NP_001171528.1:p.Ala212Ser
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NM_152830.3:c.634G>T
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NP_690043.1:p.Ala212Ser
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NM_001382700.1:c.1789G>T
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NP_001369629.1:p.Ala597Ser
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NM_001382701.1:c.1504G>T
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NP_001369630.1:p.Ala502Ser
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NM_001382702.1:c.286G>T
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NP_001369631.1:p.Ala96Ser
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NR_168483.1:n.734G>T
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