ENST00000302445.8:c.428T>C
MANE Select
|
ENSP00000303043.3:p.Ile143Thr
|
|
ENST00000302445.7:c.428T>C
|
ENSP00000303043.3:p.Ile143Thr
|
|
ENST00000319410.9:c.512T>C
|
ENSP00000325448.5:p.Ile171Thr
|
|
ENST00000562875.5:c.223-410T>C
|
ENSP00000456185.1:n.223-410T>C
|
|
ENST00000564578.5:c.346T>C
|
ENSP00000455818.1:p.Ser116Pro
|
|
ENST00000566249.5:c.230T>C
|
|
|
ENST00000566560.5:n.542T>C
|
|
|
ENST00000568378.5:c.146+7775T>C
|
ENSP00000454512.1:n.146+7775T>C
|
|
ENST00000568682.5:c.-41T>C
|
ENSP00000462057.1:n.-41T>C
|
|
ENST00000570215.1:c.512T>C
|
ENSP00000458028.1:p.Ile171Thr
|
|
NM_001130089.1:c.512T>C , LRG_366t1:c.512T>C
|
NP_001123561.1:p.Ile171Thr
|
|
NM_005548.2:c.428T>C
|
NP_005539.1:p.Ile143Thr
|
|
XM_017023217.1:c.-41T>C
|
XP_016878706.1:n.-41T>C
|
|
NM_001130089.2:c.512T>C
|
NP_001123561.1:p.Ile171Thr
|
|
NM_001378148.1:c.-41T>C
|
NP_001365077.1:n.-41T>C
|
|
NM_005548.3:c.428T>C
MANE Select
|
NP_005539.1:p.Ile143Thr
|
|