|
NM_000138.5:c.6835G>C
MANE Select
|
NP_000129.3:p.Gly2279Arg
|
|
ENST00000316623.10:c.6835G>C
MANE Select
|
ENSP00000325527.5:p.Gly2279Arg
|
|
NM_000138.4:c.6835G>C , LRG_778t1:c.6835G>C
|
NP_000129.3:p.Gly2279Arg
|
|
ENST00000316623.9:c.6835G>C
|
ENSP00000325527.5:p.Gly2279Arg
|
|
ENST00000559133.5:c.2142G>C
|
|
|
ENST00000559133.6:c.6835G>C
|
ENSP00000453958.2:p.Gly2279Arg
|
|
ENST00000560720.1:n.122G>C
|
|
|
ENST00000674301.1:c.1939G>C
|
ENSP00000501333.1:n.1939G>C
|
|
ENST00000674301.2:c.*286G>C
|
ENSP00000501333.2:n.*286G>C
|
|
ENST00000682170.1:n.444G>C
|
|