ENST00000559133.6:c.*1190G>T
|
ENSP00000453958.2:n.*1190G>T
|
|
ENST00000674301.2:c.*1895G>T
|
ENSP00000501333.2:n.*1895G>T
|
|
ENST00000682158.1:n.1763G>T
|
|
|
ENST00000682170.1:n.2563G>T
|
|
|
ENST00000682767.1:n.1679G>T
|
|
|
ENST00000316623.10:c.8382G>T
MANE Select
|
ENSP00000325527.5:p.Leu2794Phe
|
|
ENST00000674301.1:c.3548G>T
|
ENSP00000501333.1:n.3548G>T
|
|
ENST00000316623.9:c.8382G>T
|
ENSP00000325527.5:p.Leu2794Phe
|
|
ENST00000559133.5:c.3751G>T
|
|
|
ENST00000561429.1:n.637G>T
|
|
|
NM_000138.4:c.8382G>T , LRG_778t1:c.8382G>T
|
NP_000129.3:p.Leu2794Phe
|
|
NM_000138.5:c.8382G>T
MANE Select
|
NP_000129.3:p.Leu2794Phe
|
|