ENST00000296043.7:c.973T>G
MANE Select
|
ENSP00000296043.6:p.Ser325Ala
|
|
ENST00000646790.1:c.730T>G
|
ENSP00000494970.1:p.Ser244Ala
|
|
ENST00000296043.6:c.973T>G
|
ENSP00000296043.6:p.Ser325Ala
|
|
ENST00000469923.5:n.414+8211T>G
|
|
|
ENST00000486758.5:n.782T>G
|
|
|
NM_020859.3:c.973T>G
|
NP_065910.3:p.Ser325Ala
|
|
XM_005263162.3:c.973T>G
|
XP_005263219.1:p.Ser325Ala
|
|
XM_005263163.3:c.445T>G
|
XP_005263220.1:p.Ser149Ala
|
|
XM_005263164.3:c.445T>G
|
XP_005263221.1:p.Ser149Ala
|
|
XM_005263165.3:c.445T>G
|
XP_005263222.1:p.Ser149Ala
|
|
XM_006714282.2:c.868T>G
|
XP_006714345.1:p.Ser290Ala
|
|
XM_011532157.1:c.730T>G
|
XP_011530459.1:p.Ser244Ala
|
|
XM_011532158.1:c.976T>G
|
XP_011530460.1:p.Ser326Ala
|
|
XM_011532159.1:c.976T>G
|
XP_011530461.1:p.Ser326Ala
|
|
XM_011532160.1:c.598T>G
|
XP_011530462.1:p.Ser200Ala
|
|
XM_011532161.1:c.445T>G
|
XP_011530463.1:p.Ser149Ala
|
|
XM_005263163.4:c.445T>G
|
XP_005263220.1:p.Ser149Ala
|
|
XM_005263164.4:c.445T>G
|
XP_005263221.1:p.Ser149Ala
|
|
XM_005263165.5:c.445T>G
|
XP_005263222.1:p.Ser149Ala
|
|
XM_011532157.2:c.991T>G
|
XP_011530459.2:p.Ser331Ala
|
|
XM_011532158.3:c.976T>G
|
XP_011530460.1:p.Ser326Ala
|
|
XM_011532161.2:c.445T>G
|
XP_011530463.1:p.Ser149Ala
|
|
XM_017008488.1:c.871T>G
|
XP_016863977.1:p.Ser291Ala
|
|
XM_017008489.1:c.868T>G
|
XP_016863978.1:p.Ser290Ala
|
|
NM_020859.4:c.973T>G
MANE Select
|
NP_065910.3:p.Ser325Ala
|
|