ENST00000336411.7:c.749G>T
|
ENSP00000337915.3:p.Arg250Ile
|
|
ENST00000651162.1:n.184G>T
|
|
|
ENST00000651514.1:c.749G>T
MANE Select
|
ENSP00000498939.1:p.Arg250Ile
|
|
ENST00000651783.1:c.290G>T
|
ENSP00000498924.1:p.Arg97Ile
|
|
ENST00000652018.1:c.602G>T
|
ENSP00000498733.1:p.Arg201Ile
|
|
ENST00000336411.6:c.749G>T
|
ENSP00000337915.2:p.Arg250Ile
|
|
ENST00000354593.6:c.299G>T
|
ENSP00000346607.2:p.Arg100Ile
|
|
NM_001202855.2:c.746G>T
|
NP_001189784.1:p.Arg249Ile
|
|
NM_017460.5:c.749G>T
|
NP_059488.2:p.Arg250Ile
|
|
XM_011515841.1:c.749G>T
|
XP_011514143.1:p.Arg250Ile
|
|
XM_011515842.1:c.746G>T
|
XP_011514144.1:p.Arg249Ile
|
|
NM_017460.6:c.749G>T
MANE Select
|
NP_059488.2:p.Arg250Ile
|
|
NM_001202855.3:c.746G>T
|
NP_001189784.1:p.Arg249Ile
|
|