ENST00000578493.2:n.936T>C
|
|
|
ENST00000699291.1:c.728T>C
|
ENSP00000514272.1:n.728T>C
|
|
ENST00000699292.1:n.643T>C
|
|
|
ENST00000225275.4:c.1603T>C
MANE Select
|
ENSP00000225275.3:p.Trp535Arg
|
|
ENST00000225275.3:c.1603T>C
|
ENSP00000225275.3:p.Trp535Arg
|
|
ENST00000577220.1:c.61T>C
|
ENSP00000464668.1:p.Trp21Arg
|
|
NM_000250.1:c.1603T>C , LRG_84t1:c.1603T>C
|
NP_000241.1:p.Trp535Arg
|
|
XM_011524821.1:c.1789T>C
|
XP_011523123.1:p.Trp597Arg
|
|
XM_011524822.1:c.1318T>C
|
XP_011523124.1:p.Trp440Arg
|
|
XM_011524823.1:c.*152T>C
|
XP_011523125.1:n.*152T>C
|
|
NM_000250.2:c.1603T>C
MANE Select
|
NP_000241.1:p.Trp535Arg
|
|