ENST00000695651.1:n.1000G>A
|
|
|
ENST00000695652.1:c.2529G>A
|
ENSP00000512083.1:p.Gln843=
|
|
ENST00000695653.1:c.561G>A
|
ENSP00000512084.1:p.Gln187=
|
|
ENST00000695654.1:c.1776G>A
|
ENSP00000512085.1:p.Gln592=
|
|
ENST00000695655.1:c.1593G>A
|
ENSP00000512086.1:n.1593G>A
|
|
ENST00000695692.1:n.2016G>A
|
|
|
ENST00000245907.11:c.2652G>A
MANE Select
|
ENSP00000245907.4:p.Gln884=
|
|
ENST00000245907.10:c.2652G>A
|
ENSP00000245907.4:p.Gln884=
|
|
ENST00000594005.1:n.228G>A
|
|
|
NM_000064.3:c.2652G>A
|
NP_000055.2:p.Gln884=
|
|
NM_000064.4:c.2652G>A
MANE Select
|
NP_000055.2:p.Gln884=
|
|