ENST00000559133.6:c.*1187C=
|
ENSP00000453958.2:n.*1187C=
|
|
ENST00000674301.2:c.*1892C=
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ENSP00000501333.2:n.*1892C=
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|
ENST00000682158.1:n.1760C=
|
|
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ENST00000682170.1:n.2560C=
|
|
|
ENST00000682767.1:n.1676C=
|
|
|
ENST00000316623.10:c.8379C=
MANE Select
|
ENSP00000325527.5:p.Tyr2793=
|
|
ENST00000674301.1:c.3545C=
|
ENSP00000501333.1:n.3545C=
|
|
ENST00000316623.9:c.8379C=
|
ENSP00000325527.5:p.Tyr2793=
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|
ENST00000559133.5:c.3748C=
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|
|
ENST00000561429.1:n.634C=
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|
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NM_000138.4:c.8379C= , LRG_778t1:c.8379C=
|
NP_000129.3:p.Tyr2793=
|
|
NM_000138.5:c.8379C=
MANE Select
|
NP_000129.3:p.Tyr2793=
|
|