ENST00000695850.1:n.1387C>T
|
|
|
ENST00000695852.1:n.318C>T
|
|
|
ENST00000695853.1:c.*1270C>T
|
ENSP00000512218.1:n.*1270C>T
|
|
ENST00000423902.7:c.8211C>T
MANE Select
|
ENSP00000392028.1:p.Ser2737=
|
|
ENST00000423902.6:c.8211C>T
|
ENSP00000392028.1:p.Ser2737=
|
|
ENST00000524602.5:c.2064C>T
|
ENSP00000437061.1:p.Ser688=
|
|
ENST00000528280.1:n.257C>T
|
|
|
NM_001316690.1:c.2064C>T
|
NP_001303619.1:p.Ser688=
|
|
NM_017780.3:c.8211C>T
|
NP_060250.2:p.Ser2737=
|
|
XM_011517553.1:c.8301C>T
|
XP_011515855.1:p.Ser2767=
|
|
XM_011517554.1:c.8301C>T
|
XP_011515856.1:p.Ser2767=
|
|
XM_011517555.1:c.8298C>T
|
XP_011515857.1:p.Ser2766=
|
|
XM_011517556.1:c.8079C>T
|
XP_011515858.1:p.Ser2693=
|
|
XM_011517557.1:c.6288C>T
|
XP_011515859.1:p.Ser2096=
|
|
XM_011517558.1:c.5838C>T
|
XP_011515860.1:p.Ser1946=
|
|
XM_011517559.1:c.5046C>T
|
XP_011515861.1:p.Ser1682=
|
|
XM_011517553.2:c.8301C>T
|
XP_011515855.1:p.Ser2767=
|
|
XM_011517554.3:c.8301C>T
|
XP_011515856.1:p.Ser2767=
|
|
XM_011517555.2:c.8298C>T
|
XP_011515857.1:p.Ser2766=
|
|
XM_017013612.1:c.8301C>T
|
XP_016869101.1:p.Ser2767=
|
|
XM_017013613.1:c.8208C>T
|
XP_016869102.1:p.Ser2736=
|
|
NM_017780.4:c.8211C>T
MANE Select
|
NP_060250.2:p.Ser2737=
|
|