ENST00000695850.1:n.1428C>T
|
|
|
ENST00000695852.1:n.359C>T
|
|
|
ENST00000695853.1:c.*1311C>T
|
ENSP00000512218.1:n.*1311C>T
|
|
ENST00000423902.7:c.8252C>T
MANE Select
|
ENSP00000392028.1:p.Ala2751Val
|
|
ENST00000423902.6:c.8252C>T
|
ENSP00000392028.1:p.Ala2751Val
|
|
ENST00000524602.5:c.2105C>T
|
ENSP00000437061.1:p.Ala702Val
|
|
ENST00000528280.1:n.298C>T
|
|
|
NM_001316690.1:c.2105C>T
|
NP_001303619.1:p.Ala702Val
|
|
NM_017780.3:c.8252C>T
|
NP_060250.2:p.Ala2751Val
|
|
XM_011517553.1:c.8342C>T
|
XP_011515855.1:p.Ala2781Val
|
|
XM_011517554.1:c.8342C>T
|
XP_011515856.1:p.Ala2781Val
|
|
XM_011517555.1:c.8339C>T
|
XP_011515857.1:p.Ala2780Val
|
|
XM_011517556.1:c.8120C>T
|
XP_011515858.1:p.Ala2707Val
|
|
XM_011517557.1:c.6329C>T
|
XP_011515859.1:p.Ala2110Val
|
|
XM_011517558.1:c.5879C>T
|
XP_011515860.1:p.Ala1960Val
|
|
XM_011517559.1:c.5087C>T
|
XP_011515861.1:p.Ala1696Val
|
|
XM_011517553.2:c.8342C>T
|
XP_011515855.1:p.Ala2781Val
|
|
XM_011517554.3:c.8342C>T
|
XP_011515856.1:p.Ala2781Val
|
|
XM_011517555.2:c.8339C>T
|
XP_011515857.1:p.Ala2780Val
|
|
XM_017013612.1:c.8342C>T
|
XP_016869101.1:p.Ala2781Val
|
|
XM_017013613.1:c.8249C>T
|
XP_016869102.1:p.Ala2750Val
|
|
NM_017780.4:c.8252C>T
MANE Select
|
NP_060250.2:p.Ala2751Val
|
|