ENST00000559133.6:c.*1107A>T
|
ENSP00000453958.2:n.*1107A>T
|
|
ENST00000674301.2:c.*1812A>T
|
ENSP00000501333.2:n.*1812A>T
|
|
ENST00000682158.1:n.1680A>T
|
|
|
ENST00000682170.1:n.2480A>T
|
|
|
ENST00000682767.1:n.1596A>T
|
|
|
ENST00000316623.10:c.8299A>T
MANE Select
|
ENSP00000325527.5:p.Asn2767Tyr
|
|
ENST00000674301.1:c.3465A>T
|
ENSP00000501333.1:n.3465A>T
|
|
ENST00000316623.9:c.8299A>T
|
ENSP00000325527.5:p.Asn2767Tyr
|
|
ENST00000559133.5:c.3668A>T
|
|
|
ENST00000561429.1:n.554A>T
|
|
|
NM_000138.4:c.8299A>T , LRG_778t1:c.8299A>T
|
NP_000129.3:p.Asn2767Tyr
|
|
NM_000138.5:c.8299A>T
MANE Select
|
NP_000129.3:p.Asn2767Tyr
|
|