ENST00000578493.2:n.872C>G
|
|
|
ENST00000699291.1:c.664C>G
|
ENSP00000514272.1:n.664C>G
|
|
ENST00000699292.1:n.579C>G
|
|
|
ENST00000225275.4:c.1539C>G
MANE Select
|
ENSP00000225275.3:p.Asp513Glu
|
|
ENST00000225275.3:c.1539C>G
|
ENSP00000225275.3:p.Asp513Glu
|
|
NM_000250.1:c.1539C>G , LRG_84t1:c.1539C>G
|
NP_000241.1:p.Asp513Glu
|
|
XM_011524821.1:c.1725C>G
|
XP_011523123.1:p.Asp575Glu
|
|
XM_011524822.1:c.1254C>G
|
XP_011523124.1:p.Asp418Glu
|
|
XM_011524823.1:c.*88C>G
|
XP_011523125.1:n.*88C>G
|
|
NM_000250.2:c.1539C>G
MANE Select
|
NP_000241.1:p.Asp513Glu
|
|