ENST00000559133.6:c.*738G>C
|
ENSP00000453958.2:n.*738G>C
|
|
ENST00000674301.2:c.*1443G>C
|
ENSP00000501333.2:n.*1443G>C
|
|
ENST00000682158.1:n.1311G>C
|
|
|
ENST00000682170.1:n.2111G>C
|
|
|
ENST00000682767.1:n.1227G>C
|
|
|
ENST00000316623.10:c.7930G>C
MANE Select
|
ENSP00000325527.5:p.Gly2644Arg
|
|
ENST00000674301.1:c.3096G>C
|
ENSP00000501333.1:n.3096G>C
|
|
ENST00000316623.9:c.7930G>C
|
ENSP00000325527.5:p.Gly2644Arg
|
|
ENST00000559133.5:c.3299G>C
|
|
|
ENST00000561429.1:n.185G>C
|
|
|
NM_000138.4:c.7930G>C , LRG_778t1:c.7930G>C
|
NP_000129.3:p.Gly2644Arg
|
|
NM_000138.5:c.7930G>C
MANE Select
|
NP_000129.3:p.Gly2644Arg
|
|