ENST00000269228.10:c.3324G=
MANE Select
|
ENSP00000269228.4:p.Ala1108=
|
|
ENST00000269228.9:c.3324G=
|
ENSP00000269228.4:p.Ala1108=
|
|
ENST00000586150.5:c.79G=
|
|
|
ENST00000588867.1:n.79G=
|
|
|
ENST00000591051.1:c.2402G=
|
|
|
ENST00000591107.6:c.1G=
|
|
|
NM_000271.4:c.3324G=
|
NP_000262.2:p.Ala1108=
|
|
XM_005258277.1:c.3375G=
|
XP_005258334.1:p.Ala1125=
|
|
XM_005258278.3:c.3375G=
|
XP_005258335.1:p.Ala1125=
|
|
XM_005258279.1:c.3324G=
|
XP_005258336.1:p.Ala1108=
|
|
XM_006722479.2:c.3375G=
|
XP_006722542.1:p.Ala1125=
|
|
XM_011526015.1:c.2910G=
|
XP_011524317.1:p.Ala970=
|
|
XM_005258278.5:c.3375G=
|
XP_005258335.1:p.Ala1125=
|
|
XM_005258279.2:c.3324G=
|
XP_005258336.1:p.Ala1108=
|
|
XM_006722479.3:c.3375G=
|
XP_006722542.1:p.Ala1125=
|
|
XM_017025784.1:c.3375G=
|
XP_016881273.1:p.Ala1125=
|
|
XM_017025785.1:c.3375G=
|
XP_016881274.1:p.Ala1125=
|
|
XM_017025786.1:c.3324G=
|
XP_016881275.1:p.Ala1108=
|
|
XM_017025787.1:c.3324G=
|
XP_016881276.1:p.Ala1108=
|
|
NM_000271.5:c.3324G=
MANE Select
|
NP_000262.2:p.Ala1108=
|
|