ENST00000695850.1:n.1436G>C
|
|
|
ENST00000695852.1:n.367G>C
|
|
|
ENST00000695853.1:c.*1319G>C
|
ENSP00000512218.1:n.*1319G>C
|
|
ENST00000423902.7:c.8260G>C
MANE Select
|
ENSP00000392028.1:p.Asp2754His
|
|
ENST00000423902.6:c.8260G>C
|
ENSP00000392028.1:p.Asp2754His
|
|
ENST00000524602.5:c.2113G>C
|
ENSP00000437061.1:p.Asp705His
|
|
ENST00000528280.1:n.306G>C
|
|
|
NM_001316690.1:c.2113G>C
|
NP_001303619.1:p.Asp705His
|
|
NM_017780.3:c.8260G>C
|
NP_060250.2:p.Asp2754His
|
|
XM_011517553.1:c.8350G>C
|
XP_011515855.1:p.Asp2784His
|
|
XM_011517554.1:c.8350G>C
|
XP_011515856.1:p.Asp2784His
|
|
XM_011517555.1:c.8347G>C
|
XP_011515857.1:p.Asp2783His
|
|
XM_011517556.1:c.8128G>C
|
XP_011515858.1:p.Asp2710His
|
|
XM_011517557.1:c.6337G>C
|
XP_011515859.1:p.Asp2113His
|
|
XM_011517558.1:c.5887G>C
|
XP_011515860.1:p.Asp1963His
|
|
XM_011517559.1:c.5095G>C
|
XP_011515861.1:p.Asp1699His
|
|
XM_011517553.2:c.8350G>C
|
XP_011515855.1:p.Asp2784His
|
|
XM_011517554.3:c.8350G>C
|
XP_011515856.1:p.Asp2784His
|
|
XM_011517555.2:c.8347G>C
|
XP_011515857.1:p.Asp2783His
|
|
XM_017013612.1:c.8350G>C
|
XP_016869101.1:p.Asp2784His
|
|
XM_017013613.1:c.8257G>C
|
XP_016869102.1:p.Asp2753His
|
|
NM_017780.4:c.8260G>C
MANE Select
|
NP_060250.2:p.Asp2754His
|
|