ENST00000578493.2:n.754A>T
|
|
|
ENST00000699291.1:c.546A>T
|
ENSP00000514272.1:p.Glu182Asp
|
|
ENST00000699292.1:n.461A>T
|
|
|
ENST00000225275.4:c.1421A>T
MANE Select
|
ENSP00000225275.3:p.Lys474Met
|
|
ENST00000225275.3:c.1421A>T
|
ENSP00000225275.3:p.Lys474Met
|
|
NM_000250.1:c.1421A>T , LRG_84t1:c.1421A>T
|
NP_000241.1:p.Lys474Met
|
|
XM_011524821.1:c.1607A>T
|
XP_011523123.1:p.Lys536Met
|
|
XM_011524822.1:c.1136A>T
|
XP_011523124.1:p.Lys379Met
|
|
XM_011524823.1:c.1446A>T
|
XP_011523125.1:p.Glu482Asp
|
|
NM_000250.2:c.1421A>T
MANE Select
|
NP_000241.1:p.Lys474Met
|
|