ENST00000371270.6:c.1351A>T
MANE Select
|
ENSP00000360317.3:p.Thr451Ser
|
|
ENST00000371270.5:c.1351A>T
|
ENSP00000360317.3:p.Thr451Ser
|
|
ENST00000490994.6:c.*1137A>T
|
ENSP00000433314.1:n.*1137A>T
|
|
ENST00000525991.5:c.*926A>T
|
ENSP00000433842.1:n.*926A>T
|
|
ENST00000526814.5:n.1606A>T
|
|
|
ENST00000527420.5:c.*208A>T
|
ENSP00000433191.1:n.*208A>T
|
|
ENST00000527953.5:n.1645A>T
|
|
|
ENST00000531714.1:n.539A>T
|
|
|
ENST00000533320.5:n.1585A>T
|
|
|
ENST00000535898.5:c.1045A>T
|
ENSP00000445062.1:p.Thr349Ser
|
|
ENST00000539050.5:c.1141A>T
|
ENSP00000442343.2:p.Thr381Ser
|
|
ENST00000623108.3:c.1141A>T
|
ENSP00000485110.1:p.Thr381Ser
|
|
NM_000770.3:c.1351A>T
MANE Select
|
NP_000761.3:p.Thr451Ser
|
|
NM_001198853.1:c.1141A>T
|
NP_001185782.1:p.Thr381Ser
|
|
NM_001198854.1:c.1045A>T
|
NP_001185783.1:p.Thr349Ser
|
|
NM_001198855.1:c.1141A>T
|
NP_001185784.1:p.Thr381Ser
|
|
XR_945610.1:n.1486A>T
|
|
|