ENST00000695850.1:n.1672T>A
|
|
|
ENST00000695852.1:n.603T>A
|
|
|
ENST00000695853.1:c.*1555T>A
|
ENSP00000512218.1:n.*1555T>A
|
|
ENST00000423902.7:c.8496T>A
MANE Select
|
ENSP00000392028.1:p.Ser2832Arg
|
|
ENST00000423902.6:c.8496T>A
|
ENSP00000392028.1:p.Ser2832Arg
|
|
ENST00000524602.5:c.2349T>A
|
ENSP00000437061.1:p.Ser783Arg
|
|
ENST00000528280.1:n.542T>A
|
|
|
NM_001316690.1:c.2349T>A
|
NP_001303619.1:p.Ser783Arg
|
|
NM_017780.3:c.8496T>A
|
NP_060250.2:p.Ser2832Arg
|
|
XM_011517553.1:c.8586T>A
|
XP_011515855.1:p.Ser2862Arg
|
|
XM_011517554.1:c.8586T>A
|
XP_011515856.1:p.Ser2862Arg
|
|
XM_011517555.1:c.8583T>A
|
XP_011515857.1:p.Ser2861Arg
|
|
XM_011517556.1:c.8364T>A
|
XP_011515858.1:p.Ser2788Arg
|
|
XM_011517557.1:c.6573T>A
|
XP_011515859.1:p.Ser2191Arg
|
|
XM_011517558.1:c.6123T>A
|
XP_011515860.1:p.Ser2041Arg
|
|
XM_011517559.1:c.5331T>A
|
XP_011515861.1:p.Ser1777Arg
|
|
XM_011517553.2:c.8586T>A
|
XP_011515855.1:p.Ser2862Arg
|
|
XM_011517554.3:c.8586T>A
|
XP_011515856.1:p.Ser2862Arg
|
|
XM_011517555.2:c.8583T>A
|
XP_011515857.1:p.Ser2861Arg
|
|
XM_017013612.1:c.8586T>A
|
XP_016869101.1:p.Ser2862Arg
|
|
XM_017013613.1:c.8493T>A
|
XP_016869102.1:p.Ser2831Arg
|
|
NM_017780.4:c.8496T>A
MANE Select
|
NP_060250.2:p.Ser2832Arg
|
|