ENST00000695850.1:n.1733G>A
|
|
|
ENST00000695852.1:n.664G>A
|
|
|
ENST00000695853.1:c.*1616G>A
|
ENSP00000512218.1:n.*1616G>A
|
|
ENST00000423902.7:c.8557G>A
MANE Select
|
ENSP00000392028.1:p.Glu2853Lys
|
|
ENST00000423902.6:c.8557G>A
|
ENSP00000392028.1:p.Glu2853Lys
|
|
ENST00000524602.5:c.2410G>A
|
ENSP00000437061.1:p.Glu804Lys
|
|
NM_001316690.1:c.2410G>A
|
NP_001303619.1:p.Glu804Lys
|
|
NM_017780.3:c.8557G>A
|
NP_060250.2:p.Glu2853Lys
|
|
XM_011517553.1:c.8647G>A
|
XP_011515855.1:p.Glu2883Lys
|
|
XM_011517554.1:c.8647G>A
|
XP_011515856.1:p.Glu2883Lys
|
|
XM_011517555.1:c.8644G>A
|
XP_011515857.1:p.Glu2882Lys
|
|
XM_011517556.1:c.8425G>A
|
XP_011515858.1:p.Glu2809Lys
|
|
XM_011517557.1:c.6634G>A
|
XP_011515859.1:p.Glu2212Lys
|
|
XM_011517558.1:c.6184G>A
|
XP_011515860.1:p.Glu2062Lys
|
|
XM_011517559.1:c.5392G>A
|
XP_011515861.1:p.Glu1798Lys
|
|
XM_011517553.2:c.8647G>A
|
XP_011515855.1:p.Glu2883Lys
|
|
XM_011517554.3:c.8647G>A
|
XP_011515856.1:p.Glu2883Lys
|
|
XM_011517555.2:c.8644G>A
|
XP_011515857.1:p.Glu2882Lys
|
|
XM_017013612.1:c.8647G>A
|
XP_016869101.1:p.Glu2883Lys
|
|
XM_017013613.1:c.8554G>A
|
XP_016869102.1:p.Glu2852Lys
|
|
NM_017780.4:c.8557G>A
MANE Select
|
NP_060250.2:p.Glu2853Lys
|
|