ENST00000578493.2:n.731G>C
|
|
|
ENST00000699291.1:c.523G>C
|
ENSP00000514272.1:p.Ala175Pro
|
|
ENST00000699292.1:n.438G>C
|
|
|
ENST00000225275.4:c.1398G>C
MANE Select
|
ENSP00000225275.3:p.Val466=
|
|
ENST00000225275.3:c.1398G>C
|
ENSP00000225275.3:p.Val466=
|
|
NM_000250.1:c.1398G>C , LRG_84t1:c.1398G>C
|
NP_000241.1:p.Val466=
|
|
XM_011524821.1:c.1584G>C
|
XP_011523123.1:p.Val528=
|
|
XM_011524822.1:c.1113G>C
|
XP_011523124.1:p.Val371=
|
|
XM_011524823.1:c.1423G>C
|
XP_011523125.1:p.Ala475Pro
|
|
NM_000250.2:c.1398G>C
MANE Select
|
NP_000241.1:p.Val466=
|
|