ENST00000673739.2:c.*2732G>T
|
ENSP00000501110.2:n.*2732G>T
|
|
ENST00000673882.2:c.*2521G>T
|
ENSP00000501253.2:n.*2521G>T
|
|
ENST00000673739.1:c.3140G>T
|
ENSP00000501110.1:n.3140G>T
|
|
ENST00000673882.1:c.2929G>T
|
ENSP00000501253.1:n.2929G>T
|
|
ENST00000233242.5:c.3426G>T
MANE Select
|
ENSP00000233242.1:p.Ser1142=
|
|
ENST00000616098.4:c.3426G>T
|
ENSP00000477990.1:p.Ser1142=
|
|
NM_000384.2:c.3426G>T
|
NP_000375.2:p.Ser1142=
|
|
XM_011532809.1:c.3426G>T
|
XP_011531111.1:p.Ser1142=
|
|
NM_000384.3:c.3426G>T
MANE Select
|
NP_000375.3:p.Ser1142=
|
|