ENST00000578493.2:n.705A>G
|
|
|
ENST00000699291.1:c.497A>G
|
ENSP00000514272.1:p.His166Arg
|
|
ENST00000699292.1:n.412A>G
|
|
|
ENST00000225275.4:c.1372A>G
MANE Select
|
ENSP00000225275.3:p.Thr458Ala
|
|
ENST00000225275.3:c.1372A>G
|
ENSP00000225275.3:p.Thr458Ala
|
|
NM_000250.1:c.1372A>G , LRG_84t1:c.1372A>G
|
NP_000241.1:p.Thr458Ala
|
|
XM_011524821.1:c.1558A>G
|
XP_011523123.1:p.Thr520Ala
|
|
XM_011524822.1:c.1087A>G
|
XP_011523124.1:p.Thr363Ala
|
|
XM_011524823.1:c.1397A>G
|
XP_011523125.1:p.His466Arg
|
|
NM_000250.2:c.1372A>G
MANE Select
|
NP_000241.1:p.Thr458Ala
|
|