ENST00000695850.1:n.1398T>G
|
|
|
ENST00000695852.1:n.329T>G
|
|
|
ENST00000695853.1:c.*1281T>G
|
ENSP00000512218.1:n.*1281T>G
|
|
ENST00000423902.7:c.8222T>G
MANE Select
|
ENSP00000392028.1:p.Ile2741Ser
|
|
ENST00000423902.6:c.8222T>G
|
ENSP00000392028.1:p.Ile2741Ser
|
|
ENST00000524602.5:c.2075T>G
|
ENSP00000437061.1:p.Ile692Ser
|
|
ENST00000528280.1:n.268T>G
|
|
|
NM_001316690.1:c.2075T>G
|
NP_001303619.1:p.Ile692Ser
|
|
NM_017780.3:c.8222T>G
|
NP_060250.2:p.Ile2741Ser
|
|
XM_011517553.1:c.8312T>G
|
XP_011515855.1:p.Ile2771Ser
|
|
XM_011517554.1:c.8312T>G
|
XP_011515856.1:p.Ile2771Ser
|
|
XM_011517555.1:c.8309T>G
|
XP_011515857.1:p.Ile2770Ser
|
|
XM_011517556.1:c.8090T>G
|
XP_011515858.1:p.Ile2697Ser
|
|
XM_011517557.1:c.6299T>G
|
XP_011515859.1:p.Ile2100Ser
|
|
XM_011517558.1:c.5849T>G
|
XP_011515860.1:p.Ile1950Ser
|
|
XM_011517559.1:c.5057T>G
|
XP_011515861.1:p.Ile1686Ser
|
|
XM_011517553.2:c.8312T>G
|
XP_011515855.1:p.Ile2771Ser
|
|
XM_011517554.3:c.8312T>G
|
XP_011515856.1:p.Ile2771Ser
|
|
XM_011517555.2:c.8309T>G
|
XP_011515857.1:p.Ile2770Ser
|
|
XM_017013612.1:c.8312T>G
|
XP_016869101.1:p.Ile2771Ser
|
|
XM_017013613.1:c.8219T>G
|
XP_016869102.1:p.Ile2740Ser
|
|
NM_017780.4:c.8222T>G
MANE Select
|
NP_060250.2:p.Ile2741Ser
|
|