ENST00000695850.1:n.1352G>A
|
|
|
ENST00000695852.1:n.283G>A
|
|
|
ENST00000695853.1:c.*1235G>A
|
ENSP00000512218.1:n.*1235G>A
|
|
ENST00000423902.7:c.8176G>A
MANE Select
|
ENSP00000392028.1:p.Ala2726Thr
|
|
ENST00000423902.6:c.8176G>A
|
ENSP00000392028.1:p.Ala2726Thr
|
|
ENST00000524602.5:c.2029G>A
|
ENSP00000437061.1:p.Ala677Thr
|
|
ENST00000528280.1:n.222G>A
|
|
|
ENST00000532149.1:n.598G>A
|
|
|
ENST00000618450.1:n.4212G>A
|
|
|
NM_001316690.1:c.2029G>A
|
NP_001303619.1:p.Ala677Thr
|
|
NM_017780.3:c.8176G>A
|
NP_060250.2:p.Ala2726Thr
|
|
XM_011517553.1:c.8266G>A
|
XP_011515855.1:p.Ala2756Thr
|
|
XM_011517554.1:c.8266G>A
|
XP_011515856.1:p.Ala2756Thr
|
|
XM_011517555.1:c.8263G>A
|
XP_011515857.1:p.Ala2755Thr
|
|
XM_011517556.1:c.8044G>A
|
XP_011515858.1:p.Ala2682Thr
|
|
XM_011517557.1:c.6253G>A
|
XP_011515859.1:p.Ala2085Thr
|
|
XM_011517558.1:c.5803G>A
|
XP_011515860.1:p.Ala1935Thr
|
|
XM_011517559.1:c.5011G>A
|
XP_011515861.1:p.Ala1671Thr
|
|
XM_011517553.2:c.8266G>A
|
XP_011515855.1:p.Ala2756Thr
|
|
XM_011517554.3:c.8266G>A
|
XP_011515856.1:p.Ala2756Thr
|
|
XM_011517555.2:c.8263G>A
|
XP_011515857.1:p.Ala2755Thr
|
|
XM_017013612.1:c.8266G>A
|
XP_016869101.1:p.Ala2756Thr
|
|
XM_017013613.1:c.8173G>A
|
XP_016869102.1:p.Ala2725Thr
|
|
NM_017780.4:c.8176G>A
MANE Select
|
NP_060250.2:p.Ala2726Thr
|
|