ENST00000262493.12:c.736G=
MANE Select
|
ENSP00000262493.6:p.Glu246=
|
|
ENST00000562316.6:c.403G=
|
ENSP00000457238.2:p.Glu135=
|
|
ENST00000564727.2:c.40G=
|
ENSP00000454971.2:p.Glu14=
|
|
ENST00000568375.2:c.116-3470G=
|
|
|
ENST00000638185.1:n.951G=
|
|
|
ENST00000638210.1:n.1036G=
|
|
|
ENST00000638705.1:c.736G=
|
ENSP00000491223.1:p.Glu246=
|
|
ENST00000638836.1:n.646G=
|
|
|
ENST00000639055.1:n.1457G=
|
|
|
ENST00000639251.1:n.637G=
|
|
|
ENST00000639268.1:c.371G=
|
|
|
ENST00000639341.1:c.261G=
|
|
|
ENST00000639770.1:c.774G=
|
ENSP00000491999.1:n.774G=
|
|
ENST00000640390.1:n.666G=
|
|
|
ENST00000640469.1:c.100G=
|
ENSP00000491875.1:p.Glu34=
|
|
ENST00000640560.1:n.512G=
|
|
|
ENST00000640893.1:c.*134G=
|
ENSP00000492677.1:n.*134G=
|
|
ENST00000262493.10:c.736G=
|
ENSP00000262493.6:p.Glu246=
|
|
ENST00000568375.1:n.116-3470G=
|
|
|
NM_020988.2:c.736G=
|
NP_066268.1:p.Glu246=
|
|
XM_011523003.1:c.610G=
|
XP_011521305.1:p.Glu204=
|
|
XM_011523003.3:c.610G=
|
XP_011521305.1:p.Glu204=
|
|
NM_020988.3:c.736G=
MANE Select
|
NP_066268.1:p.Glu246=
|
|