ENST00000695850.1:n.1360A>C
|
|
|
ENST00000695852.1:n.291A>C
|
|
|
ENST00000695853.1:c.*1243A>C
|
ENSP00000512218.1:n.*1243A>C
|
|
ENST00000423902.7:c.8184A>C
MANE Select
|
ENSP00000392028.1:p.Ala2728=
|
|
ENST00000423902.6:c.8184A>C
|
ENSP00000392028.1:p.Ala2728=
|
|
ENST00000524602.5:c.2037A>C
|
ENSP00000437061.1:p.Ala679=
|
|
ENST00000528280.1:n.230A>C
|
|
|
ENST00000532149.1:n.606A>C
|
|
|
ENST00000618450.1:n.4220A>C
|
|
|
NM_001316690.1:c.2037A>C
|
NP_001303619.1:p.Ala679=
|
|
NM_017780.3:c.8184A>C
|
NP_060250.2:p.Ala2728=
|
|
XM_011517553.1:c.8274A>C
|
XP_011515855.1:p.Ala2758=
|
|
XM_011517554.1:c.8274A>C
|
XP_011515856.1:p.Ala2758=
|
|
XM_011517555.1:c.8271A>C
|
XP_011515857.1:p.Ala2757=
|
|
XM_011517556.1:c.8052A>C
|
XP_011515858.1:p.Ala2684=
|
|
XM_011517557.1:c.6261A>C
|
XP_011515859.1:p.Ala2087=
|
|
XM_011517558.1:c.5811A>C
|
XP_011515860.1:p.Ala1937=
|
|
XM_011517559.1:c.5019A>C
|
XP_011515861.1:p.Ala1673=
|
|
XM_011517553.2:c.8274A>C
|
XP_011515855.1:p.Ala2758=
|
|
XM_011517554.3:c.8274A>C
|
XP_011515856.1:p.Ala2758=
|
|
XM_011517555.2:c.8271A>C
|
XP_011515857.1:p.Ala2757=
|
|
XM_017013612.1:c.8274A>C
|
XP_016869101.1:p.Ala2758=
|
|
XM_017013613.1:c.8181A>C
|
XP_016869102.1:p.Ala2727=
|
|
NM_017780.4:c.8184A>C
MANE Select
|
NP_060250.2:p.Ala2728=
|
|