ENST00000559133.6:c.6778G>C
|
ENSP00000453958.2:p.Glu2260Gln
|
|
ENST00000674301.2:c.*229G>C
|
ENSP00000501333.2:n.*229G>C
|
|
ENST00000682170.1:n.387G>C
|
|
|
ENST00000316623.10:c.6778G>C
MANE Select
|
ENSP00000325527.5:p.Glu2260Gln
|
|
ENST00000674301.1:c.1882G>C
|
ENSP00000501333.1:n.1882G>C
|
|
ENST00000316623.9:c.6778G>C
|
ENSP00000325527.5:p.Glu2260Gln
|
|
ENST00000537463.6:c.*2541G>C
|
ENSP00000440294.2:n.*2541G>C
|
|
ENST00000559133.5:c.2085G>C
|
|
|
ENST00000560720.1:n.65G>C
|
|
|
NM_000138.4:c.6778G>C , LRG_778t1:c.6778G>C
|
NP_000129.3:p.Glu2260Gln
|
|
NM_000138.5:c.6778G>C
MANE Select
|
NP_000129.3:p.Glu2260Gln
|
|