ENST00000695850.1:n.1429T>C
|
|
|
ENST00000695852.1:n.360T>C
|
|
|
ENST00000695853.1:c.*1312T>C
|
ENSP00000512218.1:n.*1312T>C
|
|
ENST00000423902.7:c.8253T>C
MANE Select
|
ENSP00000392028.1:p.Ala2751=
|
|
ENST00000423902.6:c.8253T>C
|
ENSP00000392028.1:p.Ala2751=
|
|
ENST00000524602.5:c.2106T>C
|
ENSP00000437061.1:p.Ala702=
|
|
ENST00000528280.1:n.299T>C
|
|
|
NM_001316690.1:c.2106T>C
|
NP_001303619.1:p.Ala702=
|
|
NM_017780.3:c.8253T>C
|
NP_060250.2:p.Ala2751=
|
|
XM_011517553.1:c.8343T>C
|
XP_011515855.1:p.Ala2781=
|
|
XM_011517554.1:c.8343T>C
|
XP_011515856.1:p.Ala2781=
|
|
XM_011517555.1:c.8340T>C
|
XP_011515857.1:p.Ala2780=
|
|
XM_011517556.1:c.8121T>C
|
XP_011515858.1:p.Ala2707=
|
|
XM_011517557.1:c.6330T>C
|
XP_011515859.1:p.Ala2110=
|
|
XM_011517558.1:c.5880T>C
|
XP_011515860.1:p.Ala1960=
|
|
XM_011517559.1:c.5088T>C
|
XP_011515861.1:p.Ala1696=
|
|
XM_011517553.2:c.8343T>C
|
XP_011515855.1:p.Ala2781=
|
|
XM_011517554.3:c.8343T>C
|
XP_011515856.1:p.Ala2781=
|
|
XM_011517555.2:c.8340T>C
|
XP_011515857.1:p.Ala2780=
|
|
XM_017013612.1:c.8343T>C
|
XP_016869101.1:p.Ala2781=
|
|
XM_017013613.1:c.8250T>C
|
XP_016869102.1:p.Ala2750=
|
|
NM_017780.4:c.8253T>C
MANE Select
|
NP_060250.2:p.Ala2751=
|
|