ENST00000578493.2:n.815C>G
|
|
|
ENST00000699291.1:c.607C>G
|
ENSP00000514272.1:n.607C>G
|
|
ENST00000699292.1:n.522C>G
|
|
|
ENST00000225275.4:c.1482C>G
MANE Select
|
ENSP00000225275.3:p.Phe494Leu
|
|
ENST00000225275.3:c.1482C>G
|
ENSP00000225275.3:p.Phe494Leu
|
|
NM_000250.1:c.1482C>G , LRG_84t1:c.1482C>G
|
NP_000241.1:p.Phe494Leu
|
|
XM_011524821.1:c.1668C>G
|
XP_011523123.1:p.Phe556Leu
|
|
XM_011524822.1:c.1197C>G
|
XP_011523124.1:p.Phe399Leu
|
|
XM_011524823.1:c.*31C>G
|
XP_011523125.1:n.*31C>G
|
|
NM_000250.2:c.1482C>G
MANE Select
|
NP_000241.1:p.Phe494Leu
|
|