ENST00000262493.12:c.754G=
MANE Select
|
ENSP00000262493.6:p.Asp252=
|
|
ENST00000562316.6:c.421G=
|
ENSP00000457238.2:p.Asp141=
|
|
ENST00000564727.2:c.58G=
|
ENSP00000454971.2:p.Asp20=
|
|
ENST00000568375.2:c.116-3452G=
|
|
|
ENST00000638185.1:n.969G=
|
|
|
ENST00000638210.1:n.1054G=
|
|
|
ENST00000638705.1:c.754G=
|
ENSP00000491223.1:p.Asp252=
|
|
ENST00000638836.1:n.664G=
|
|
|
ENST00000639055.1:n.1475G=
|
|
|
ENST00000639251.1:n.655G=
|
|
|
ENST00000639268.1:c.389G=
|
|
|
ENST00000639341.1:c.279G=
|
|
|
ENST00000639770.1:c.792G=
|
ENSP00000491999.1:n.792G=
|
|
ENST00000640390.1:n.684G=
|
|
|
ENST00000640469.1:c.118G=
|
ENSP00000491875.1:p.Asp40=
|
|
ENST00000640560.1:n.530G=
|
|
|
ENST00000640893.1:c.*152G=
|
ENSP00000492677.1:n.*152G=
|
|
ENST00000262493.10:c.754G=
|
ENSP00000262493.6:p.Asp252=
|
|
ENST00000568375.1:n.116-3452G=
|
|
|
NM_020988.2:c.754G=
|
NP_066268.1:p.Asp252=
|
|
XM_011523003.1:c.628G=
|
XP_011521305.1:p.Asp210=
|
|
XM_011523003.3:c.628G=
|
XP_011521305.1:p.Asp210=
|
|
NM_020988.3:c.754G=
MANE Select
|
NP_066268.1:p.Asp252=
|
|