ENST00000371270.6:c.*86G>T
MANE Select
|
ENSP00000360317.3:n.*86G>T
|
|
ENST00000371270.5:c.*86G>T
|
ENSP00000360317.3:n.*86G>T
|
|
ENST00000490994.6:c.*1345G>T
|
ENSP00000433314.1:n.*1345G>T
|
|
ENST00000525991.5:c.*1134G>T
|
ENSP00000433842.1:n.*1134G>T
|
|
ENST00000526814.5:n.1814G>T
|
|
|
ENST00000527420.5:c.*416G>T
|
ENSP00000433191.1:n.*416G>T
|
|
ENST00000527953.5:n.1853G>T
|
|
|
ENST00000533320.5:n.1793G>T
|
|
|
ENST00000535898.5:c.*86G>T
|
ENSP00000445062.1:n.*86G>T
|
|
ENST00000539050.5:c.*86G>T
|
ENSP00000442343.2:n.*86G>T
|
|
ENST00000623108.3:c.*86G>T
|
ENSP00000485110.1:n.*86G>T
|
|
NM_000770.3:c.*86G>T
MANE Select
|
NP_000761.3:n.*86G>T
|
|
NM_001198853.1:c.*86G>T
|
NP_001185782.1:n.*86G>T
|
|
NM_001198854.1:c.*86G>T
|
NP_001185783.1:n.*86G>T
|
|
NM_001198855.1:c.*86G>T
|
NP_001185784.1:n.*86G>T
|
|