ENST00000559133.6:c.*873G>C
|
ENSP00000453958.2:n.*873G>C
|
|
ENST00000674301.2:c.*1578G>C
|
ENSP00000501333.2:n.*1578G>C
|
|
ENST00000682158.1:n.1446G>C
|
|
|
ENST00000682170.1:n.2246G>C
|
|
|
ENST00000682767.1:n.1362G>C
|
|
|
ENST00000316623.10:c.8065G>C
MANE Select
|
ENSP00000325527.5:p.Gly2689Arg
|
|
ENST00000674301.1:c.3231G>C
|
ENSP00000501333.1:n.3231G>C
|
|
ENST00000316623.9:c.8065G>C
|
ENSP00000325527.5:p.Gly2689Arg
|
|
ENST00000559133.5:c.3434G>C
|
|
|
ENST00000561429.1:n.320G>C
|
|
|
NM_000138.4:c.8065G>C , LRG_778t1:c.8065G>C
|
NP_000129.3:p.Gly2689Arg
|
|
NM_000138.5:c.8065G>C
MANE Select
|
NP_000129.3:p.Gly2689Arg
|
|