ENST00000695850.1:n.1378T>C
|
|
|
ENST00000695852.1:n.309T>C
|
|
|
ENST00000695853.1:c.*1261T>C
|
ENSP00000512218.1:n.*1261T>C
|
|
ENST00000423902.7:c.8202T>C
MANE Select
|
ENSP00000392028.1:p.Ala2734=
|
|
ENST00000423902.6:c.8202T>C
|
ENSP00000392028.1:p.Ala2734=
|
|
ENST00000524602.5:c.2055T>C
|
ENSP00000437061.1:p.Ala685=
|
|
ENST00000528280.1:n.248T>C
|
|
|
NM_001316690.1:c.2055T>C
|
NP_001303619.1:p.Ala685=
|
|
NM_017780.3:c.8202T>C
|
NP_060250.2:p.Ala2734=
|
|
XM_011517553.1:c.8292T>C
|
XP_011515855.1:p.Ala2764=
|
|
XM_011517554.1:c.8292T>C
|
XP_011515856.1:p.Ala2764=
|
|
XM_011517555.1:c.8289T>C
|
XP_011515857.1:p.Ala2763=
|
|
XM_011517556.1:c.8070T>C
|
XP_011515858.1:p.Ala2690=
|
|
XM_011517557.1:c.6279T>C
|
XP_011515859.1:p.Ala2093=
|
|
XM_011517558.1:c.5829T>C
|
XP_011515860.1:p.Ala1943=
|
|
XM_011517559.1:c.5037T>C
|
XP_011515861.1:p.Ala1679=
|
|
XM_011517553.2:c.8292T>C
|
XP_011515855.1:p.Ala2764=
|
|
XM_011517554.3:c.8292T>C
|
XP_011515856.1:p.Ala2764=
|
|
XM_011517555.2:c.8289T>C
|
XP_011515857.1:p.Ala2763=
|
|
XM_017013612.1:c.8292T>C
|
XP_016869101.1:p.Ala2764=
|
|
XM_017013613.1:c.8199T>C
|
XP_016869102.1:p.Ala2733=
|
|
NM_017780.4:c.8202T>C
MANE Select
|
NP_060250.2:p.Ala2734=
|
|