ENST00000578493.2:n.1119C>G
|
|
|
ENST00000699291.1:c.911C>G
|
ENSP00000514272.1:n.911C>G
|
|
ENST00000699292.1:n.1321C>G
|
|
|
ENST00000225275.4:c.1786C>G
MANE Select
|
ENSP00000225275.3:p.Leu596Val
|
|
ENST00000225275.3:c.1786C>G
|
ENSP00000225275.3:p.Leu596Val
|
|
ENST00000577220.1:c.183+61C>G
|
ENSP00000464668.1:n.183+61C>G
|
|
NM_000250.1:c.1786C>G , LRG_84t1:c.1786C>G
|
NP_000241.1:p.Leu596Val
|
|
XM_011524821.1:c.1972C>G
|
XP_011523123.1:p.Leu658Val
|
|
XM_011524822.1:c.1501C>G
|
XP_011523124.1:p.Leu501Val
|
|
NM_000250.2:c.1786C>G
MANE Select
|
NP_000241.1:p.Leu596Val
|
|