ENST00000388958.8:c.1294T>A
|
ENSP00000373610.3:p.Ser432Thr
|
|
ENST00000646100.2:c.1294T>A
MANE Select
|
ENSP00000496564.2:p.Ser432Thr
|
|
ENST00000647277.1:c.*108T>A
|
ENSP00000495594.1:n.*108T>A
|
|
ENST00000286149.8:c.1336T>A
|
ENSP00000286149.4:p.Ser446Thr
|
|
ENST00000388956.8:c.1057T>A
|
ENSP00000373608.4:p.Ser353Thr
|
|
ENST00000388957.3:c.322T>A
|
ENSP00000373609.3:p.Ser108Thr
|
|
ENST00000388958.7:c.1294T>A
|
ENSP00000373610.3:p.Ser432Thr
|
|
ENST00000563871.5:n.514T>A
|
|
|
NM_001161683.1:c.1057T>A
|
NP_001155155.1:p.Ser353Thr
|
|
NM_144672.3:c.1294T>A
|
NP_653273.3:p.Ser432Thr
|
|
NM_170664.2:c.322T>A
|
NP_733764.1:p.Ser108Thr
|
|
XM_011545747.1:c.1294T>A
|
XP_011544049.1:p.Ser432Thr
|
|
XM_011545748.1:c.163T>A
|
XP_011544050.1:p.Ser55Thr
|
|
NM_144672.4:c.1294T>A
MANE Select
|
NP_653273.3:p.Ser432Thr
|
|
XM_011545748.2:c.163T>A
|
XP_011544050.2:p.Ser55Thr
|
|
XR_002957775.1:n.389T>A
|
|
|
NM_001161683.2:c.1057T>A
|
NP_001155155.1:p.Ser353Thr
|
|
NM_170664.3:c.322T>A
|
NP_733764.1:p.Ser108Thr
|
|