ENST00000297289.9:c.987T>A
|
ENSP00000516619.1:p.Thr329=
|
|
ENST00000418964.2:c.2085T>A
|
ENSP00000389424.2:p.Thr695=
|
|
ENST00000706906.1:c.*2054T>A
|
ENSP00000516618.1:n.*2054T>A
|
|
ENST00000308192.14:c.2034T>A
MANE Select
|
ENSP00000308938.9:p.Thr678=
|
|
ENST00000308192.13:c.2034T>A
|
ENSP00000308938.9:p.Thr678=
|
|
ENST00000461414.2:n.57T>A
|
|
|
ENST00000467466.1:n.335T>A
|
|
|
NM_000301.3:c.2034T>A , LRG_571t1:c.2034T>A
|
NP_000292.1:p.Thr678=
|
|
NM_000301.4:c.2034T>A
|
NP_000292.1:p.Thr678=
|
|
NM_000301.5:c.2034T>A
MANE Select
|
NP_000292.1:p.Thr678=
|
|