ENST00000559133.6:c.*387G>A
|
ENSP00000453958.2:n.*387G>A
|
|
ENST00000674301.2:c.*1092G>A
|
ENSP00000501333.2:n.*1092G>A
|
|
ENST00000682170.1:n.1760G>A
|
|
|
ENST00000682767.1:n.876G>A
|
|
|
ENST00000316623.10:c.7579G>A
MANE Select
|
ENSP00000325527.5:p.Glu2527Lys
|
|
ENST00000674301.1:c.2745G>A
|
ENSP00000501333.1:n.2745G>A
|
|
ENST00000316623.9:c.7579G>A
|
ENSP00000325527.5:p.Glu2527Lys
|
|
ENST00000559133.5:c.2948G>A
|
|
|
NM_000138.4:c.7579G>A , LRG_778t1:c.7579G>A
|
NP_000129.3:p.Glu2527Lys
|
|
NM_000138.5:c.7579G>A
MANE Select
|
NP_000129.3:p.Glu2527Lys
|
|