ENST00000697124.1:n.1748G>T
|
|
|
ENST00000219596.6:c.*281G>T
MANE Select
|
ENSP00000219596.1:n.*281G>T
|
|
ENST00000219596.5:c.*281G>T
|
ENSP00000219596.1:n.*281G>T
|
|
ENST00000339854.8:c.*281G>T
|
ENSP00000339639.4:n.*281G>T
|
|
ENST00000536980.5:c.*903G>T
|
ENSP00000444178.1:n.*903G>T
|
|
ENST00000537682.5:c.*903G>T
|
ENSP00000438611.1:n.*903G>T
|
|
ENST00000538326.5:c.*1252G>T
|
ENSP00000437486.1:n.*1252G>T
|
|
ENST00000542898.5:c.*903G>T
|
ENSP00000444615.1:n.*903G>T
|
|
NM_000243.2:c.*281G>T , LRG_190t1:c.*281G>T
|
NP_000234.1:n.*281G>T
|
|
NM_001198536.1:c.*831G>T
|
NP_001185465.1:n.*831G>T
|
|
NM_000243.3:c.*281G>T
MANE Select
|
NP_000234.1:n.*281G>T
|
|
NM_001198536.2:c.*831G>T
|
NP_001185465.2:n.*831G>T
|
|