ENST00000559133.6:c.*1166T>C
|
ENSP00000453958.2:n.*1166T>C
|
|
ENST00000674301.2:c.*1871T>C
|
ENSP00000501333.2:n.*1871T>C
|
|
ENST00000682158.1:n.1739T>C
|
|
|
ENST00000682170.1:n.2539T>C
|
|
|
ENST00000682767.1:n.1655T>C
|
|
|
ENST00000316623.10:c.8358T>C
MANE Select
|
ENSP00000325527.5:p.Thr2786=
|
|
ENST00000674301.1:c.3524T>C
|
ENSP00000501333.1:n.3524T>C
|
|
ENST00000316623.9:c.8358T>C
|
ENSP00000325527.5:p.Thr2786=
|
|
ENST00000559133.5:c.3727T>C
|
|
|
ENST00000561429.1:n.613T>C
|
|
|
NM_000138.4:c.8358T>C , LRG_778t1:c.8358T>C
|
NP_000129.3:p.Thr2786=
|
|
NM_000138.5:c.8358T>C
MANE Select
|
NP_000129.3:p.Thr2786=
|
|