ENST00000697124.1:n.1675G>T
|
|
|
ENST00000219596.6:c.*208G>T
MANE Select
|
ENSP00000219596.1:n.*208G>T
|
|
ENST00000219596.5:c.*208G>T
|
ENSP00000219596.1:n.*208G>T
|
|
ENST00000339854.8:c.*208G>T
|
ENSP00000339639.4:n.*208G>T
|
|
ENST00000536980.5:c.*830G>T
|
ENSP00000444178.1:n.*830G>T
|
|
ENST00000537682.5:c.*830G>T
|
ENSP00000438611.1:n.*830G>T
|
|
ENST00000538326.5:c.*1179G>T
|
ENSP00000437486.1:n.*1179G>T
|
|
ENST00000542898.5:c.*830G>T
|
ENSP00000444615.1:n.*830G>T
|
|
NM_000243.2:c.*208G>T , LRG_190t1:c.*208G>T
|
NP_000234.1:n.*208G>T
|
|
NM_001198536.1:c.*758G>T
|
NP_001185465.1:n.*758G>T
|
|
NM_000243.3:c.*208G>T
MANE Select
|
NP_000234.1:n.*208G>T
|
|
NM_001198536.2:c.*758G>T
|
NP_001185465.2:n.*758G>T
|
|