ENST00000578493.2:n.784A>T
|
|
|
ENST00000699291.1:c.576A>T
|
ENSP00000514272.1:p.Ter192Cys
|
|
ENST00000699292.1:n.491A>T
|
|
|
ENST00000225275.4:c.1451A>T
MANE Select
|
ENSP00000225275.3:p.Asp484Val
|
|
ENST00000225275.3:c.1451A>T
|
ENSP00000225275.3:p.Asp484Val
|
|
NM_000250.1:c.1451A>T , LRG_84t1:c.1451A>T
|
NP_000241.1:p.Asp484Val
|
|
XM_011524821.1:c.1637A>T
|
XP_011523123.1:p.Asp546Val
|
|
XM_011524822.1:c.1166A>T
|
XP_011523124.1:p.Asp389Val
|
|
XM_011524823.1:c.1476A>T
|
XP_011523125.1:p.Ter492Cys
|
|
NM_000250.2:c.1451A>T
MANE Select
|
NP_000241.1:p.Asp484Val
|
|