ENST00000559133.6:c.*380T>C
|
ENSP00000453958.2:n.*380T>C
|
|
ENST00000674301.2:c.*1085T>C
|
ENSP00000501333.2:n.*1085T>C
|
|
ENST00000682170.1:n.1753T>C
|
|
|
ENST00000682767.1:n.869T>C
|
|
|
ENST00000316623.10:c.7572T>C
MANE Select
|
ENSP00000325527.5:p.Asp2524=
|
|
ENST00000674301.1:c.2738T>C
|
ENSP00000501333.1:n.2738T>C
|
|
ENST00000316623.9:c.7572T>C
|
ENSP00000325527.5:p.Asp2524=
|
|
ENST00000559133.5:c.2941T>C
|
|
|
NM_000138.4:c.7572T>C , LRG_778t1:c.7572T>C
|
NP_000129.3:p.Asp2524=
|
|
NM_000138.5:c.7572T>C
MANE Select
|
NP_000129.3:p.Asp2524=
|
|