ENST00000336411.7:c.1385T>C
|
ENSP00000337915.3:p.Ile462Thr
|
|
ENST00000651162.1:n.727T>C
|
|
|
ENST00000651514.1:c.1292T>C
MANE Select
|
ENSP00000498939.1:p.Ile431Thr
|
|
ENST00000651783.1:c.833T>C
|
ENSP00000498924.1:p.Ile278Thr
|
|
ENST00000652018.1:c.1145T>C
|
ENSP00000498733.1:p.Ile382Thr
|
|
ENST00000336411.6:c.1292T>C
|
ENSP00000337915.2:p.Ile431Thr
|
|
ENST00000354593.6:c.842T>C
|
ENSP00000346607.2:p.Ile281Thr
|
|
NM_001202855.2:c.1289T>C
|
NP_001189784.1:p.Ile430Thr
|
|
NM_017460.5:c.1292T>C
|
NP_059488.2:p.Ile431Thr
|
|
XM_011515841.1:c.1385T>C
|
XP_011514143.1:p.Ile462Thr
|
|
XM_011515842.1:c.1382T>C
|
XP_011514144.1:p.Ile461Thr
|
|
NM_017460.6:c.1292T>C
MANE Select
|
NP_059488.2:p.Ile431Thr
|
|
NM_001202855.3:c.1289T>C
|
NP_001189784.1:p.Ile430Thr
|
|