ENST00000695850.1:n.1345T>C
|
|
|
ENST00000695852.1:n.276T>C
|
|
|
ENST00000695853.1:c.*1228T>C
|
ENSP00000512218.1:n.*1228T>C
|
|
ENST00000423902.7:c.8169T>C
MANE Select
|
ENSP00000392028.1:p.Ser2723=
|
|
ENST00000423902.6:c.8169T>C
|
ENSP00000392028.1:p.Ser2723=
|
|
ENST00000524602.5:c.2022T>C
|
ENSP00000437061.1:p.Ser674=
|
|
ENST00000528280.1:n.215T>C
|
|
|
ENST00000532149.1:n.591T>C
|
|
|
ENST00000618450.1:n.4205T>C
|
|
|
NM_001316690.1:c.2022T>C
|
NP_001303619.1:p.Ser674=
|
|
NM_017780.3:c.8169T>C
|
NP_060250.2:p.Ser2723=
|
|
XM_011517553.1:c.8259T>C
|
XP_011515855.1:p.Ser2753=
|
|
XM_011517554.1:c.8259T>C
|
XP_011515856.1:p.Ser2753=
|
|
XM_011517555.1:c.8256T>C
|
XP_011515857.1:p.Ser2752=
|
|
XM_011517556.1:c.8037T>C
|
XP_011515858.1:p.Ser2679=
|
|
XM_011517557.1:c.6246T>C
|
XP_011515859.1:p.Ser2082=
|
|
XM_011517558.1:c.5796T>C
|
XP_011515860.1:p.Ser1932=
|
|
XM_011517559.1:c.5004T>C
|
XP_011515861.1:p.Ser1668=
|
|
XM_011517553.2:c.8259T>C
|
XP_011515855.1:p.Ser2753=
|
|
XM_011517554.3:c.8259T>C
|
XP_011515856.1:p.Ser2753=
|
|
XM_011517555.2:c.8256T>C
|
XP_011515857.1:p.Ser2752=
|
|
XM_017013612.1:c.8259T>C
|
XP_016869101.1:p.Ser2753=
|
|
XM_017013613.1:c.8166T>C
|
XP_016869102.1:p.Ser2722=
|
|
NM_017780.4:c.8169T>C
MANE Select
|
NP_060250.2:p.Ser2723=
|
|