ENST00000695850.1:n.1385T>G
|
|
|
ENST00000695852.1:n.316T>G
|
|
|
ENST00000695853.1:c.*1268T>G
|
ENSP00000512218.1:n.*1268T>G
|
|
ENST00000423902.7:c.8209T>G
MANE Select
|
ENSP00000392028.1:p.Ser2737Ala
|
|
ENST00000423902.6:c.8209T>G
|
ENSP00000392028.1:p.Ser2737Ala
|
|
ENST00000524602.5:c.2062T>G
|
ENSP00000437061.1:p.Ser688Ala
|
|
ENST00000528280.1:n.255T>G
|
|
|
NM_001316690.1:c.2062T>G
|
NP_001303619.1:p.Ser688Ala
|
|
NM_017780.3:c.8209T>G
|
NP_060250.2:p.Ser2737Ala
|
|
XM_011517553.1:c.8299T>G
|
XP_011515855.1:p.Ser2767Ala
|
|
XM_011517554.1:c.8299T>G
|
XP_011515856.1:p.Ser2767Ala
|
|
XM_011517555.1:c.8296T>G
|
XP_011515857.1:p.Ser2766Ala
|
|
XM_011517556.1:c.8077T>G
|
XP_011515858.1:p.Ser2693Ala
|
|
XM_011517557.1:c.6286T>G
|
XP_011515859.1:p.Ser2096Ala
|
|
XM_011517558.1:c.5836T>G
|
XP_011515860.1:p.Ser1946Ala
|
|
XM_011517559.1:c.5044T>G
|
XP_011515861.1:p.Ser1682Ala
|
|
XM_011517553.2:c.8299T>G
|
XP_011515855.1:p.Ser2767Ala
|
|
XM_011517554.3:c.8299T>G
|
XP_011515856.1:p.Ser2767Ala
|
|
XM_011517555.2:c.8296T>G
|
XP_011515857.1:p.Ser2766Ala
|
|
XM_017013612.1:c.8299T>G
|
XP_016869101.1:p.Ser2767Ala
|
|
XM_017013613.1:c.8206T>G
|
XP_016869102.1:p.Ser2736Ala
|
|
NM_017780.4:c.8209T>G
MANE Select
|
NP_060250.2:p.Ser2737Ala
|
|