ENST00000302068.9:c.1092A=
MANE Select
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ENSP00000306099.4:p.Glu364=
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ENST00000302068.8:c.1092A=
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ENSP00000306099.4:p.Glu364=
|
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ENST00000502545.5:n.939+340A=
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|
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ENST00000509493.1:c.435A=
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ENSP00000426757.1:p.Glu145=
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NM_001184741.1:c.915A=
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NP_001171670.1:p.Glu305=
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NM_005141.4:c.1092A= , LRG_558t1:c.1092A=
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NP_005132.2:p.Glu364=
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NM_001382759.1:c.960A=
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NP_001369688.1:p.Glu320=
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NM_001382760.1:c.1092A=
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NP_001369689.1:p.Glu364=
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NM_001382761.1:c.1092A=
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NP_001369690.1:p.Glu364=
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NM_001382762.1:c.792A=
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NP_001369691.1:p.Glu264=
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NM_001382763.1:c.1083A=
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NP_001369692.1:p.Glu361=
|
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NM_001382764.1:c.1080+12A=
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NP_001369693.1:n.1080+12A=
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NM_001382765.1:c.1092A=
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NP_001369694.1:p.Glu364=
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NM_005141.5:c.1092A=
MANE Select
|
NP_005132.2:p.Glu364=
|
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