ENST00000695850.1:n.1496G>A
|
|
|
ENST00000695852.1:n.427G>A
|
|
|
ENST00000695853.1:c.*1379G>A
|
ENSP00000512218.1:n.*1379G>A
|
|
ENST00000423902.7:c.8320G>A
MANE Select
|
ENSP00000392028.1:p.Gly2774Ser
|
|
ENST00000423902.6:c.8320G>A
|
ENSP00000392028.1:p.Gly2774Ser
|
|
ENST00000524602.5:c.2173G>A
|
ENSP00000437061.1:p.Gly725Ser
|
|
ENST00000528280.1:n.366G>A
|
|
|
NM_001316690.1:c.2173G>A
|
NP_001303619.1:p.Gly725Ser
|
|
NM_017780.3:c.8320G>A
|
NP_060250.2:p.Gly2774Ser
|
|
XM_011517553.1:c.8410G>A
|
XP_011515855.1:p.Gly2804Ser
|
|
XM_011517554.1:c.8410G>A
|
XP_011515856.1:p.Gly2804Ser
|
|
XM_011517555.1:c.8407G>A
|
XP_011515857.1:p.Gly2803Ser
|
|
XM_011517556.1:c.8188G>A
|
XP_011515858.1:p.Gly2730Ser
|
|
XM_011517557.1:c.6397G>A
|
XP_011515859.1:p.Gly2133Ser
|
|
XM_011517558.1:c.5947G>A
|
XP_011515860.1:p.Gly1983Ser
|
|
XM_011517559.1:c.5155G>A
|
XP_011515861.1:p.Gly1719Ser
|
|
XM_011517553.2:c.8410G>A
|
XP_011515855.1:p.Gly2804Ser
|
|
XM_011517554.3:c.8410G>A
|
XP_011515856.1:p.Gly2804Ser
|
|
XM_011517555.2:c.8407G>A
|
XP_011515857.1:p.Gly2803Ser
|
|
XM_017013612.1:c.8410G>A
|
XP_016869101.1:p.Gly2804Ser
|
|
XM_017013613.1:c.8317G>A
|
XP_016869102.1:p.Gly2773Ser
|
|
NM_017780.4:c.8320G>A
MANE Select
|
NP_060250.2:p.Gly2774Ser
|
|