ENST00000695850.1:n.1427G>A
|
|
|
ENST00000695852.1:n.358G>A
|
|
|
ENST00000695853.1:c.*1310G>A
|
ENSP00000512218.1:n.*1310G>A
|
|
ENST00000423902.7:c.8251G>A
MANE Select
|
ENSP00000392028.1:p.Ala2751Thr
|
|
ENST00000423902.6:c.8251G>A
|
ENSP00000392028.1:p.Ala2751Thr
|
|
ENST00000524602.5:c.2104G>A
|
ENSP00000437061.1:p.Ala702Thr
|
|
ENST00000528280.1:n.297G>A
|
|
|
NM_001316690.1:c.2104G>A
|
NP_001303619.1:p.Ala702Thr
|
|
NM_017780.3:c.8251G>A
|
NP_060250.2:p.Ala2751Thr
|
|
XM_011517553.1:c.8341G>A
|
XP_011515855.1:p.Ala2781Thr
|
|
XM_011517554.1:c.8341G>A
|
XP_011515856.1:p.Ala2781Thr
|
|
XM_011517555.1:c.8338G>A
|
XP_011515857.1:p.Ala2780Thr
|
|
XM_011517556.1:c.8119G>A
|
XP_011515858.1:p.Ala2707Thr
|
|
XM_011517557.1:c.6328G>A
|
XP_011515859.1:p.Ala2110Thr
|
|
XM_011517558.1:c.5878G>A
|
XP_011515860.1:p.Ala1960Thr
|
|
XM_011517559.1:c.5086G>A
|
XP_011515861.1:p.Ala1696Thr
|
|
XM_011517553.2:c.8341G>A
|
XP_011515855.1:p.Ala2781Thr
|
|
XM_011517554.3:c.8341G>A
|
XP_011515856.1:p.Ala2781Thr
|
|
XM_011517555.2:c.8338G>A
|
XP_011515857.1:p.Ala2780Thr
|
|
XM_017013612.1:c.8341G>A
|
XP_016869101.1:p.Ala2781Thr
|
|
XM_017013613.1:c.8248G>A
|
XP_016869102.1:p.Ala2750Thr
|
|
NM_017780.4:c.8251G>A
MANE Select
|
NP_060250.2:p.Ala2751Thr
|
|