ENST00000695850.1:n.810T>C
|
|
|
ENST00000695851.1:n.14T>C
|
|
|
ENST00000695853.1:c.*693T>C
|
ENSP00000512218.1:n.*693T>C
|
|
ENST00000423902.7:c.7634T>C
MANE Select
|
ENSP00000392028.1:p.Phe2545Ser
|
|
ENST00000423902.6:c.7634T>C
|
ENSP00000392028.1:p.Phe2545Ser
|
|
ENST00000524602.5:c.1717-1300T>C
|
ENSP00000437061.1:n.1717-1300T>C
|
|
ENST00000531695.1:n.58T>C
|
|
|
ENST00000618450.1:n.26T>C
|
|
|
NM_001316690.1:c.1717-1300T>C
|
NP_001303619.1:n.1717-1300T>C
|
|
NM_017780.3:c.7634T>C
|
NP_060250.2:p.Phe2545Ser
|
|
XM_011517553.1:c.7724T>C
|
XP_011515855.1:p.Phe2575Ser
|
|
XM_011517554.1:c.7724T>C
|
XP_011515856.1:p.Phe2575Ser
|
|
XM_011517555.1:c.7721T>C
|
XP_011515857.1:p.Phe2574Ser
|
|
XM_011517556.1:c.7699-1267T>C
|
XP_011515858.1:n.7699-1267T>C
|
|
XM_011517557.1:c.5711T>C
|
XP_011515859.1:p.Phe1904Ser
|
|
XM_011517558.1:c.5261T>C
|
XP_011515860.1:p.Phe1754Ser
|
|
XM_011517559.1:c.4469T>C
|
XP_011515861.1:p.Phe1490Ser
|
|
XM_011517553.2:c.7724T>C
|
XP_011515855.1:p.Phe2575Ser
|
|
XM_011517554.3:c.7724T>C
|
XP_011515856.1:p.Phe2575Ser
|
|
XM_011517555.2:c.7721T>C
|
XP_011515857.1:p.Phe2574Ser
|
|
XM_017013612.1:c.7724T>C
|
XP_016869101.1:p.Phe2575Ser
|
|
XM_017013613.1:c.7631T>C
|
XP_016869102.1:p.Phe2544Ser
|
|
NM_017780.4:c.7634T>C
MANE Select
|
NP_060250.2:p.Phe2545Ser
|
|