ENST00000695850.1:n.1364G>T
|
|
|
ENST00000695852.1:n.295G>T
|
|
|
ENST00000695853.1:c.*1247G>T
|
ENSP00000512218.1:n.*1247G>T
|
|
ENST00000423902.7:c.8188G>T
MANE Select
|
ENSP00000392028.1:p.Ala2730Ser
|
|
ENST00000423902.6:c.8188G>T
|
ENSP00000392028.1:p.Ala2730Ser
|
|
ENST00000524602.5:c.2041G>T
|
ENSP00000437061.1:p.Ala681Ser
|
|
ENST00000528280.1:n.234G>T
|
|
|
ENST00000532149.1:n.610G>T
|
|
|
NM_001316690.1:c.2041G>T
|
NP_001303619.1:p.Ala681Ser
|
|
NM_017780.3:c.8188G>T
|
NP_060250.2:p.Ala2730Ser
|
|
XM_011517553.1:c.8278G>T
|
XP_011515855.1:p.Ala2760Ser
|
|
XM_011517554.1:c.8278G>T
|
XP_011515856.1:p.Ala2760Ser
|
|
XM_011517555.1:c.8275G>T
|
XP_011515857.1:p.Ala2759Ser
|
|
XM_011517556.1:c.8056G>T
|
XP_011515858.1:p.Ala2686Ser
|
|
XM_011517557.1:c.6265G>T
|
XP_011515859.1:p.Ala2089Ser
|
|
XM_011517558.1:c.5815G>T
|
XP_011515860.1:p.Ala1939Ser
|
|
XM_011517559.1:c.5023G>T
|
XP_011515861.1:p.Ala1675Ser
|
|
XM_011517553.2:c.8278G>T
|
XP_011515855.1:p.Ala2760Ser
|
|
XM_011517554.3:c.8278G>T
|
XP_011515856.1:p.Ala2760Ser
|
|
XM_011517555.2:c.8275G>T
|
XP_011515857.1:p.Ala2759Ser
|
|
XM_017013612.1:c.8278G>T
|
XP_016869101.1:p.Ala2760Ser
|
|
XM_017013613.1:c.8185G>T
|
XP_016869102.1:p.Ala2729Ser
|
|
NM_017780.4:c.8188G>T
MANE Select
|
NP_060250.2:p.Ala2730Ser
|
|