ENST00000695850.1:n.1645T>C
|
|
|
ENST00000695852.1:n.576T>C
|
|
|
ENST00000695853.1:c.*1528T>C
|
ENSP00000512218.1:n.*1528T>C
|
|
ENST00000423902.7:c.8469T>C
MANE Select
|
ENSP00000392028.1:p.Ala2823=
|
|
ENST00000423902.6:c.8469T>C
|
ENSP00000392028.1:p.Ala2823=
|
|
ENST00000524602.5:c.2322T>C
|
ENSP00000437061.1:p.Ala774=
|
|
ENST00000528280.1:n.515T>C
|
|
|
NM_001316690.1:c.2322T>C
|
NP_001303619.1:p.Ala774=
|
|
NM_017780.3:c.8469T>C
|
NP_060250.2:p.Ala2823=
|
|
XM_011517553.1:c.8559T>C
|
XP_011515855.1:p.Ala2853=
|
|
XM_011517554.1:c.8559T>C
|
XP_011515856.1:p.Ala2853=
|
|
XM_011517555.1:c.8556T>C
|
XP_011515857.1:p.Ala2852=
|
|
XM_011517556.1:c.8337T>C
|
XP_011515858.1:p.Ala2779=
|
|
XM_011517557.1:c.6546T>C
|
XP_011515859.1:p.Ala2182=
|
|
XM_011517558.1:c.6096T>C
|
XP_011515860.1:p.Ala2032=
|
|
XM_011517559.1:c.5304T>C
|
XP_011515861.1:p.Ala1768=
|
|
XM_011517553.2:c.8559T>C
|
XP_011515855.1:p.Ala2853=
|
|
XM_011517554.3:c.8559T>C
|
XP_011515856.1:p.Ala2853=
|
|
XM_011517555.2:c.8556T>C
|
XP_011515857.1:p.Ala2852=
|
|
XM_017013612.1:c.8559T>C
|
XP_016869101.1:p.Ala2853=
|
|
XM_017013613.1:c.8466T>C
|
XP_016869102.1:p.Ala2822=
|
|
NM_017780.4:c.8469T>C
MANE Select
|
NP_060250.2:p.Ala2823=
|
|