ENST00000336411.7:c.1444A>T
|
ENSP00000337915.3:p.Asn482Tyr
|
|
ENST00000651162.1:n.786A>T
|
|
|
ENST00000651514.1:c.1351A>T
MANE Select
|
ENSP00000498939.1:p.Asn451Tyr
|
|
ENST00000651783.1:c.892A>T
|
ENSP00000498924.1:p.Asn298Tyr
|
|
ENST00000652018.1:c.1204A>T
|
ENSP00000498733.1:p.Asn402Tyr
|
|
ENST00000336411.6:c.1351A>T
|
ENSP00000337915.2:p.Asn451Tyr
|
|
ENST00000354593.6:c.901A>T
|
ENSP00000346607.2:p.Asn301Tyr
|
|
NM_001202855.2:c.1348A>T
|
NP_001189784.1:p.Asn450Tyr
|
|
NM_017460.5:c.1351A>T
|
NP_059488.2:p.Asn451Tyr
|
|
XM_011515841.1:c.1444A>T
|
XP_011514143.1:p.Asn482Tyr
|
|
XM_011515842.1:c.1441A>T
|
XP_011514144.1:p.Asn481Tyr
|
|
NM_017460.6:c.1351A>T
MANE Select
|
NP_059488.2:p.Asn451Tyr
|
|
NM_001202855.3:c.1348A>T
|
NP_001189784.1:p.Asn450Tyr
|
|