ENST00000578493.2:n.750A>T
|
|
|
ENST00000699291.1:c.542A>T
|
ENSP00000514272.1:p.Glu181Val
|
|
ENST00000699292.1:n.457A>T
|
|
|
ENST00000225275.4:c.1417A>T
MANE Select
|
ENSP00000225275.3:p.Arg473Trp
|
|
ENST00000225275.3:c.1417A>T
|
ENSP00000225275.3:p.Arg473Trp
|
|
NM_000250.1:c.1417A>T , LRG_84t1:c.1417A>T
|
NP_000241.1:p.Arg473Trp
|
|
XM_011524821.1:c.1603A>T
|
XP_011523123.1:p.Arg535Trp
|
|
XM_011524822.1:c.1132A>T
|
XP_011523124.1:p.Arg378Trp
|
|
XM_011524823.1:c.1442A>T
|
XP_011523125.1:p.Glu481Val
|
|
NM_000250.2:c.1417A>T
MANE Select
|
NP_000241.1:p.Arg473Trp
|
|