ENST00000559133.6:c.*349G>T
|
ENSP00000453958.2:n.*349G>T
|
|
ENST00000674301.2:c.*1054G>T
|
ENSP00000501333.2:n.*1054G>T
|
|
ENST00000682170.1:n.1722G>T
|
|
|
ENST00000682767.1:n.838G>T
|
|
|
ENST00000316623.10:c.7541G>T
MANE Select
|
ENSP00000325527.5:p.Gly2514Val
|
|
ENST00000674301.1:c.2707G>T
|
ENSP00000501333.1:n.2707G>T
|
|
ENST00000316623.9:c.7541G>T
|
ENSP00000325527.5:p.Gly2514Val
|
|
ENST00000559133.5:c.2910G>T
|
|
|
NM_000138.4:c.7541G>T , LRG_778t1:c.7541G>T
|
NP_000129.3:p.Gly2514Val
|
|
NM_000138.5:c.7541G>T
MANE Select
|
NP_000129.3:p.Gly2514Val
|
|