ENST00000578493.2:n.792G>T
|
|
|
ENST00000699291.1:c.584G>T
|
ENSP00000514272.1:n.584G>T
|
|
ENST00000699292.1:n.499G>T
|
|
|
ENST00000225275.4:c.1459G>T
MANE Select
|
ENSP00000225275.3:p.Asp487Tyr
|
|
ENST00000225275.3:c.1459G>T
|
ENSP00000225275.3:p.Asp487Tyr
|
|
NM_000250.1:c.1459G>T , LRG_84t1:c.1459G>T
|
NP_000241.1:p.Asp487Tyr
|
|
XM_011524821.1:c.1645G>T
|
XP_011523123.1:p.Asp549Tyr
|
|
XM_011524822.1:c.1174G>T
|
XP_011523124.1:p.Asp392Tyr
|
|
XM_011524823.1:c.*8G>T
|
XP_011523125.1:n.*8G>T
|
|
NM_000250.2:c.1459G>T
MANE Select
|
NP_000241.1:p.Asp487Tyr
|
|