ENST00000695850.1:n.1373G>T
|
|
|
ENST00000695852.1:n.304G>T
|
|
|
ENST00000695853.1:c.*1256G>T
|
ENSP00000512218.1:n.*1256G>T
|
|
ENST00000423902.7:c.8197G>T
MANE Select
|
ENSP00000392028.1:p.Ala2733Ser
|
|
ENST00000423902.6:c.8197G>T
|
ENSP00000392028.1:p.Ala2733Ser
|
|
ENST00000524602.5:c.2050G>T
|
ENSP00000437061.1:p.Ala684Ser
|
|
ENST00000528280.1:n.243G>T
|
|
|
NM_001316690.1:c.2050G>T
|
NP_001303619.1:p.Ala684Ser
|
|
NM_017780.3:c.8197G>T
|
NP_060250.2:p.Ala2733Ser
|
|
XM_011517553.1:c.8287G>T
|
XP_011515855.1:p.Ala2763Ser
|
|
XM_011517554.1:c.8287G>T
|
XP_011515856.1:p.Ala2763Ser
|
|
XM_011517555.1:c.8284G>T
|
XP_011515857.1:p.Ala2762Ser
|
|
XM_011517556.1:c.8065G>T
|
XP_011515858.1:p.Ala2689Ser
|
|
XM_011517557.1:c.6274G>T
|
XP_011515859.1:p.Ala2092Ser
|
|
XM_011517558.1:c.5824G>T
|
XP_011515860.1:p.Ala1942Ser
|
|
XM_011517559.1:c.5032G>T
|
XP_011515861.1:p.Ala1678Ser
|
|
XM_011517553.2:c.8287G>T
|
XP_011515855.1:p.Ala2763Ser
|
|
XM_011517554.3:c.8287G>T
|
XP_011515856.1:p.Ala2763Ser
|
|
XM_011517555.2:c.8284G>T
|
XP_011515857.1:p.Ala2762Ser
|
|
XM_017013612.1:c.8287G>T
|
XP_016869101.1:p.Ala2763Ser
|
|
XM_017013613.1:c.8194G>T
|
XP_016869102.1:p.Ala2732Ser
|
|
NM_017780.4:c.8197G>T
MANE Select
|
NP_060250.2:p.Ala2733Ser
|
|