ENST00000695850.1:n.1333A>C
|
|
|
ENST00000695852.1:n.264A>C
|
|
|
ENST00000695853.1:c.*1216A>C
|
ENSP00000512218.1:n.*1216A>C
|
|
ENST00000423902.7:c.8157A>C
MANE Select
|
ENSP00000392028.1:p.Arg2719Ser
|
|
ENST00000423902.6:c.8157A>C
|
ENSP00000392028.1:p.Arg2719Ser
|
|
ENST00000524602.5:c.2010A>C
|
ENSP00000437061.1:p.Arg670Ser
|
|
ENST00000528280.1:n.203A>C
|
|
|
ENST00000532149.1:n.579A>C
|
|
|
ENST00000618450.1:n.4193A>C
|
|
|
NM_001316690.1:c.2010A>C
|
NP_001303619.1:p.Arg670Ser
|
|
NM_017780.3:c.8157A>C
|
NP_060250.2:p.Arg2719Ser
|
|
XM_011517553.1:c.8247A>C
|
XP_011515855.1:p.Arg2749Ser
|
|
XM_011517554.1:c.8247A>C
|
XP_011515856.1:p.Arg2749Ser
|
|
XM_011517555.1:c.8244A>C
|
XP_011515857.1:p.Arg2748Ser
|
|
XM_011517556.1:c.8025A>C
|
XP_011515858.1:p.Arg2675Ser
|
|
XM_011517557.1:c.6234A>C
|
XP_011515859.1:p.Arg2078Ser
|
|
XM_011517558.1:c.5784A>C
|
XP_011515860.1:p.Arg1928Ser
|
|
XM_011517559.1:c.4992A>C
|
XP_011515861.1:p.Arg1664Ser
|
|
XM_011517553.2:c.8247A>C
|
XP_011515855.1:p.Arg2749Ser
|
|
XM_011517554.3:c.8247A>C
|
XP_011515856.1:p.Arg2749Ser
|
|
XM_011517555.2:c.8244A>C
|
XP_011515857.1:p.Arg2748Ser
|
|
XM_017013612.1:c.8247A>C
|
XP_016869101.1:p.Arg2749Ser
|
|
XM_017013613.1:c.8154A>C
|
XP_016869102.1:p.Arg2718Ser
|
|
NM_017780.4:c.8157A>C
MANE Select
|
NP_060250.2:p.Arg2719Ser
|
|