ENST00000673739.2:c.*2774T>C
|
ENSP00000501110.2:n.*2774T>C
|
|
ENST00000673882.2:c.*2563T>C
|
ENSP00000501253.2:n.*2563T>C
|
|
ENST00000673739.1:c.3182T>C
|
ENSP00000501110.1:n.3182T>C
|
|
ENST00000673882.1:c.2971T>C
|
ENSP00000501253.1:n.2971T>C
|
|
ENST00000233242.5:c.3468T>C
MANE Select
|
ENSP00000233242.1:p.Ala1156=
|
|
ENST00000616098.4:c.3468T>C
|
ENSP00000477990.1:p.Ala1156=
|
|
NM_000384.2:c.3468T>C
|
NP_000375.2:p.Ala1156=
|
|
XM_011532809.1:c.3468T>C
|
XP_011531111.1:p.Ala1156=
|
|
NM_000384.3:c.3468T>C
MANE Select
|
NP_000375.3:p.Ala1156=
|
|