ENST00000695850.1:n.1711G>A
|
|
|
ENST00000695852.1:n.642G>A
|
|
|
ENST00000695853.1:c.*1594G>A
|
ENSP00000512218.1:n.*1594G>A
|
|
ENST00000423902.7:c.8535G>A
MANE Select
|
ENSP00000392028.1:p.Glu2845=
|
|
ENST00000423902.6:c.8535G>A
|
ENSP00000392028.1:p.Glu2845=
|
|
ENST00000524602.5:c.2388G>A
|
ENSP00000437061.1:p.Glu796=
|
|
NM_001316690.1:c.2388G>A
|
NP_001303619.1:p.Glu796=
|
|
NM_017780.3:c.8535G>A
|
NP_060250.2:p.Glu2845=
|
|
XM_011517553.1:c.8625G>A
|
XP_011515855.1:p.Glu2875=
|
|
XM_011517554.1:c.8625G>A
|
XP_011515856.1:p.Glu2875=
|
|
XM_011517555.1:c.8622G>A
|
XP_011515857.1:p.Glu2874=
|
|
XM_011517556.1:c.8403G>A
|
XP_011515858.1:p.Glu2801=
|
|
XM_011517557.1:c.6612G>A
|
XP_011515859.1:p.Glu2204=
|
|
XM_011517558.1:c.6162G>A
|
XP_011515860.1:p.Glu2054=
|
|
XM_011517559.1:c.5370G>A
|
XP_011515861.1:p.Glu1790=
|
|
XM_011517553.2:c.8625G>A
|
XP_011515855.1:p.Glu2875=
|
|
XM_011517554.3:c.8625G>A
|
XP_011515856.1:p.Glu2875=
|
|
XM_011517555.2:c.8622G>A
|
XP_011515857.1:p.Glu2874=
|
|
XM_017013612.1:c.8625G>A
|
XP_016869101.1:p.Glu2875=
|
|
XM_017013613.1:c.8532G>A
|
XP_016869102.1:p.Glu2844=
|
|
NM_017780.4:c.8535G>A
MANE Select
|
NP_060250.2:p.Glu2845=
|
|