ENST00000695850.1:n.853T>C
|
|
|
ENST00000695851.1:n.57T>C
|
|
|
ENST00000695853.1:c.*736T>C
|
ENSP00000512218.1:n.*736T>C
|
|
ENST00000423902.7:c.7677T>C
MANE Select
|
ENSP00000392028.1:p.Ser2559=
|
|
ENST00000423902.6:c.7677T>C
|
ENSP00000392028.1:p.Ser2559=
|
|
ENST00000524602.5:c.1717-1257T>C
|
ENSP00000437061.1:n.1717-1257T>C
|
|
ENST00000531695.1:n.101T>C
|
|
|
ENST00000618450.1:n.69T>C
|
|
|
NM_001316690.1:c.1717-1257T>C
|
NP_001303619.1:n.1717-1257T>C
|
|
NM_017780.3:c.7677T>C
|
NP_060250.2:p.Ser2559=
|
|
XM_011517553.1:c.7767T>C
|
XP_011515855.1:p.Ser2589=
|
|
XM_011517554.1:c.7767T>C
|
XP_011515856.1:p.Ser2589=
|
|
XM_011517555.1:c.7764T>C
|
XP_011515857.1:p.Ser2588=
|
|
XM_011517556.1:c.7699-1224T>C
|
XP_011515858.1:n.7699-1224T>C
|
|
XM_011517557.1:c.5754T>C
|
XP_011515859.1:p.Ser1918=
|
|
XM_011517558.1:c.5304T>C
|
XP_011515860.1:p.Ser1768=
|
|
XM_011517559.1:c.4512T>C
|
XP_011515861.1:p.Ser1504=
|
|
XM_011517553.2:c.7767T>C
|
XP_011515855.1:p.Ser2589=
|
|
XM_011517554.3:c.7767T>C
|
XP_011515856.1:p.Ser2589=
|
|
XM_011517555.2:c.7764T>C
|
XP_011515857.1:p.Ser2588=
|
|
XM_017013612.1:c.7767T>C
|
XP_016869101.1:p.Ser2589=
|
|
XM_017013613.1:c.7674T>C
|
XP_016869102.1:p.Ser2558=
|
|
NM_017780.4:c.7677T>C
MANE Select
|
NP_060250.2:p.Ser2559=
|
|