ENST00000695850.1:n.930C>A
|
|
|
ENST00000695851.1:n.134C>A
|
|
|
ENST00000695853.1:c.*813C>A
|
ENSP00000512218.1:n.*813C>A
|
|
ENST00000423902.7:c.7754C>A
MANE Select
|
ENSP00000392028.1:p.Ala2585Asp
|
|
ENST00000423902.6:c.7754C>A
|
ENSP00000392028.1:p.Ala2585Asp
|
|
ENST00000524602.5:c.1717-1180C>A
|
ENSP00000437061.1:n.1717-1180C>A
|
|
ENST00000531695.1:n.178C>A
|
|
|
ENST00000618450.1:n.146C>A
|
|
|
NM_001316690.1:c.1717-1180C>A
|
NP_001303619.1:n.1717-1180C>A
|
|
NM_017780.3:c.7754C>A
|
NP_060250.2:p.Ala2585Asp
|
|
XM_011517553.1:c.7844C>A
|
XP_011515855.1:p.Ala2615Asp
|
|
XM_011517554.1:c.7844C>A
|
XP_011515856.1:p.Ala2615Asp
|
|
XM_011517555.1:c.7841C>A
|
XP_011515857.1:p.Ala2614Asp
|
|
XM_011517556.1:c.7699-1147C>A
|
XP_011515858.1:n.7699-1147C>A
|
|
XM_011517557.1:c.5831C>A
|
XP_011515859.1:p.Ala1944Asp
|
|
XM_011517558.1:c.5381C>A
|
XP_011515860.1:p.Ala1794Asp
|
|
XM_011517559.1:c.4589C>A
|
XP_011515861.1:p.Ala1530Asp
|
|
XM_011517553.2:c.7844C>A
|
XP_011515855.1:p.Ala2615Asp
|
|
XM_011517554.3:c.7844C>A
|
XP_011515856.1:p.Ala2615Asp
|
|
XM_011517555.2:c.7841C>A
|
XP_011515857.1:p.Ala2614Asp
|
|
XM_017013612.1:c.7844C>A
|
XP_016869101.1:p.Ala2615Asp
|
|
XM_017013613.1:c.7751C>A
|
XP_016869102.1:p.Ala2584Asp
|
|
NM_017780.4:c.7754C>A
MANE Select
|
NP_060250.2:p.Ala2585Asp
|
|