ENST00000695850.1:n.869C>T
|
|
|
ENST00000695851.1:n.73C>T
|
|
|
ENST00000695853.1:c.*752C>T
|
ENSP00000512218.1:n.*752C>T
|
|
ENST00000423902.7:c.7693C>T
MANE Select
|
ENSP00000392028.1:p.Pro2565Ser
|
|
ENST00000423902.6:c.7693C>T
|
ENSP00000392028.1:p.Pro2565Ser
|
|
ENST00000524602.5:c.1717-1241C>T
|
ENSP00000437061.1:n.1717-1241C>T
|
|
ENST00000531695.1:n.117C>T
|
|
|
ENST00000618450.1:n.85C>T
|
|
|
NM_001316690.1:c.1717-1241C>T
|
NP_001303619.1:n.1717-1241C>T
|
|
NM_017780.3:c.7693C>T
|
NP_060250.2:p.Pro2565Ser
|
|
XM_011517553.1:c.7783C>T
|
XP_011515855.1:p.Pro2595Ser
|
|
XM_011517554.1:c.7783C>T
|
XP_011515856.1:p.Pro2595Ser
|
|
XM_011517555.1:c.7780C>T
|
XP_011515857.1:p.Pro2594Ser
|
|
XM_011517556.1:c.7699-1208C>T
|
XP_011515858.1:n.7699-1208C>T
|
|
XM_011517557.1:c.5770C>T
|
XP_011515859.1:p.Pro1924Ser
|
|
XM_011517558.1:c.5320C>T
|
XP_011515860.1:p.Pro1774Ser
|
|
XM_011517559.1:c.4528C>T
|
XP_011515861.1:p.Pro1510Ser
|
|
XM_011517553.2:c.7783C>T
|
XP_011515855.1:p.Pro2595Ser
|
|
XM_011517554.3:c.7783C>T
|
XP_011515856.1:p.Pro2595Ser
|
|
XM_011517555.2:c.7780C>T
|
XP_011515857.1:p.Pro2594Ser
|
|
XM_017013612.1:c.7783C>T
|
XP_016869101.1:p.Pro2595Ser
|
|
XM_017013613.1:c.7690C>T
|
XP_016869102.1:p.Pro2564Ser
|
|
NM_017780.4:c.7693C>T
MANE Select
|
NP_060250.2:p.Pro2565Ser
|
|