ENST00000336411.7:c.1389dup
|
ENSP00000337915.3:p.Thr464HisfsTer?
|
|
ENST00000651162.1:n.731dup
|
|
|
ENST00000651514.1:c.1296dup
MANE Select
|
ENSP00000498939.1:p.Thr433HisfsTer?
|
|
ENST00000651783.1:c.837dup
|
ENSP00000498924.1:p.Thr280HisfsTer?
|
|
ENST00000652018.1:c.1149dup
|
ENSP00000498733.1:p.Thr384HisfsTer?
|
|
ENST00000336411.6:c.1296dup
|
ENSP00000337915.2:p.Thr433HisfsTer?
|
|
ENST00000354593.6:c.846dup
|
ENSP00000346607.2:p.Thr283HisfsTer?
|
|
NM_001202855.2:c.1293dup
|
NP_001189784.1:p.Thr432HisfsTer?
|
|
NM_017460.5:c.1296dup
|
NP_059488.2:p.Thr433HisfsTer?
|
|
XM_011515841.1:c.1389dup
|
XP_011514143.1:p.Thr464HisfsTer?
|
|
XM_011515842.1:c.1386dup
|
XP_011514144.1:p.Thr463HisfsTer?
|
|
NM_017460.6:c.1296dup
MANE Select
|
NP_059488.2:p.Thr433HisfsTer?
|
|
NM_001202855.3:c.1293dup
|
NP_001189784.1:p.Thr432HisfsTer?
|
|