ENST00000695850.1:n.791G>T
|
|
|
ENST00000695853.1:c.*674G>T
|
ENSP00000512218.1:n.*674G>T
|
|
ENST00000423902.7:c.7615G>T
MANE Select
|
ENSP00000392028.1:p.Ala2539Ser
|
|
ENST00000423902.6:c.7615G>T
|
ENSP00000392028.1:p.Ala2539Ser
|
|
ENST00000524602.5:c.1717-1319G>T
|
ENSP00000437061.1:n.1717-1319G>T
|
|
ENST00000531695.1:n.39G>T
|
|
|
ENST00000618450.1:n.7G>T
|
|
|
NM_001316690.1:c.1717-1319G>T
|
NP_001303619.1:n.1717-1319G>T
|
|
NM_017780.3:c.7615G>T
|
NP_060250.2:p.Ala2539Ser
|
|
XM_011517553.1:c.7705G>T
|
XP_011515855.1:p.Ala2569Ser
|
|
XM_011517554.1:c.7705G>T
|
XP_011515856.1:p.Ala2569Ser
|
|
XM_011517555.1:c.7702G>T
|
XP_011515857.1:p.Ala2568Ser
|
|
XM_011517556.1:c.7699-1286G>T
|
XP_011515858.1:n.7699-1286G>T
|
|
XM_011517557.1:c.5692G>T
|
XP_011515859.1:p.Ala1898Ser
|
|
XM_011517558.1:c.5242G>T
|
XP_011515860.1:p.Ala1748Ser
|
|
XM_011517559.1:c.4450G>T
|
XP_011515861.1:p.Ala1484Ser
|
|
XM_011517553.2:c.7705G>T
|
XP_011515855.1:p.Ala2569Ser
|
|
XM_011517554.3:c.7705G>T
|
XP_011515856.1:p.Ala2569Ser
|
|
XM_011517555.2:c.7702G>T
|
XP_011515857.1:p.Ala2568Ser
|
|
XM_017013612.1:c.7705G>T
|
XP_016869101.1:p.Ala2569Ser
|
|
XM_017013613.1:c.7612G>T
|
XP_016869102.1:p.Ala2538Ser
|
|
NM_017780.4:c.7615G>T
MANE Select
|
NP_060250.2:p.Ala2539Ser
|
|