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NM_000138.5:c.7937G>C
MANE Select
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NP_000129.3:p.Cys2646Ser
|
|
ENST00000316623.10:c.7937G>C
MANE Select
|
ENSP00000325527.5:p.Cys2646Ser
|
|
NM_000138.4:c.7937G>C , LRG_778t1:c.7937G>C
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NP_000129.3:p.Cys2646Ser
|
|
ENST00000316623.9:c.7937G>C
|
ENSP00000325527.5:p.Cys2646Ser
|
|
ENST00000559133.5:c.3306G>C
|
|
|
ENST00000559133.6:c.*745G>C
|
ENSP00000453958.2:n.*745G>C
|
|
ENST00000561429.1:n.192G>C
|
|
|
ENST00000674301.1:c.3103G>C
|
ENSP00000501333.1:n.3103G>C
|
|
ENST00000674301.2:c.*1450G>C
|
ENSP00000501333.2:n.*1450G>C
|
|
ENST00000682158.1:n.1318G>C
|
|
|
ENST00000682170.1:n.2118G>C
|
|
|
ENST00000682767.1:n.1234G>C
|
|