ENST00000695850.1:n.833C>G
|
|
|
ENST00000695851.1:n.37C>G
|
|
|
ENST00000695853.1:c.*716C>G
|
ENSP00000512218.1:n.*716C>G
|
|
ENST00000423902.7:c.7657C>G
MANE Select
|
ENSP00000392028.1:p.Pro2553Ala
|
|
ENST00000423902.6:c.7657C>G
|
ENSP00000392028.1:p.Pro2553Ala
|
|
ENST00000524602.5:c.1717-1277C>G
|
ENSP00000437061.1:n.1717-1277C>G
|
|
ENST00000531695.1:n.81C>G
|
|
|
ENST00000618450.1:n.49C>G
|
|
|
NM_001316690.1:c.1717-1277C>G
|
NP_001303619.1:n.1717-1277C>G
|
|
NM_017780.3:c.7657C>G
|
NP_060250.2:p.Pro2553Ala
|
|
XM_011517553.1:c.7747C>G
|
XP_011515855.1:p.Pro2583Ala
|
|
XM_011517554.1:c.7747C>G
|
XP_011515856.1:p.Pro2583Ala
|
|
XM_011517555.1:c.7744C>G
|
XP_011515857.1:p.Pro2582Ala
|
|
XM_011517556.1:c.7699-1244C>G
|
XP_011515858.1:n.7699-1244C>G
|
|
XM_011517557.1:c.5734C>G
|
XP_011515859.1:p.Pro1912Ala
|
|
XM_011517558.1:c.5284C>G
|
XP_011515860.1:p.Pro1762Ala
|
|
XM_011517559.1:c.4492C>G
|
XP_011515861.1:p.Pro1498Ala
|
|
XM_011517553.2:c.7747C>G
|
XP_011515855.1:p.Pro2583Ala
|
|
XM_011517554.3:c.7747C>G
|
XP_011515856.1:p.Pro2583Ala
|
|
XM_011517555.2:c.7744C>G
|
XP_011515857.1:p.Pro2582Ala
|
|
XM_017013612.1:c.7747C>G
|
XP_016869101.1:p.Pro2583Ala
|
|
XM_017013613.1:c.7654C>G
|
XP_016869102.1:p.Pro2552Ala
|
|
NM_017780.4:c.7657C>G
MANE Select
|
NP_060250.2:p.Pro2553Ala
|
|