ENST00000578493.2:n.701C>G
|
|
|
ENST00000699291.1:c.493C>G
|
ENSP00000514272.1:p.His165Asp
|
|
ENST00000699292.1:n.408C>G
|
|
|
ENST00000225275.4:c.1368C>G
MANE Select
|
ENSP00000225275.3:p.Ile456Met
|
|
ENST00000225275.3:c.1368C>G
|
ENSP00000225275.3:p.Ile456Met
|
|
NM_000250.1:c.1368C>G , LRG_84t1:c.1368C>G
|
NP_000241.1:p.Ile456Met
|
|
XM_011524821.1:c.1554C>G
|
XP_011523123.1:p.Ile518Met
|
|
XM_011524822.1:c.1083C>G
|
XP_011523124.1:p.Ile361Met
|
|
XM_011524823.1:c.1393C>G
|
XP_011523125.1:p.His465Asp
|
|
NM_000250.2:c.1368C>G
MANE Select
|
NP_000241.1:p.Ile456Met
|
|