ENST00000559133.6:c.6726T>A
|
ENSP00000453958.2:p.Arg2242=
|
|
ENST00000674301.2:c.*177T>A
|
ENSP00000501333.2:n.*177T>A
|
|
ENST00000682170.1:n.335T>A
|
|
|
ENST00000316623.10:c.6726T>A
MANE Select
|
ENSP00000325527.5:p.Arg2242=
|
|
ENST00000674301.1:c.1830T>A
|
ENSP00000501333.1:n.1830T>A
|
|
ENST00000316623.9:c.6726T>A
|
ENSP00000325527.5:p.Arg2242=
|
|
ENST00000537463.6:c.*2489T>A
|
ENSP00000440294.2:n.*2489T>A
|
|
ENST00000559133.5:c.2033T>A
|
|
|
ENST00000560720.1:n.13T>A
|
|
|
NM_000138.4:c.6726T>A , LRG_778t1:c.6726T>A
|
NP_000129.3:p.Arg2242=
|
|
NM_000138.5:c.6726T>A
MANE Select
|
NP_000129.3:p.Arg2242=
|
|