ENST00000205402.10:c.770T>C
MANE Select
|
ENSP00000205402.3:p.Ile257Thr
|
|
ENST00000205402.9:c.770T>C
|
ENSP00000205402.3:p.Ile257Thr
|
|
ENST00000415325.5:c.*444T>C
|
ENSP00000402593.1:n.*444T>C
|
|
ENST00000417551.5:c.770T>C
|
ENSP00000390667.1:p.Ile257Thr
|
|
ENST00000437604.6:c.626T>C
|
ENSP00000387542.2:p.Ile209Thr
|
|
ENST00000440410.5:c.701T>C
|
ENSP00000417016.1:p.Ile234Thr
|
|
ENST00000451081.5:c.*513T>C
|
ENSP00000388077.1:n.*513T>C
|
|
NM_000108.4:c.770T>C
|
NP_000099.2:p.Ile257Thr
|
|
NM_001289750.1:c.473T>C
|
NP_001276679.1:p.Ile158Thr
|
|
NM_001289751.1:c.701T>C
|
NP_001276680.1:p.Ile234Thr
|
|
NM_001289752.1:c.626T>C
|
NP_001276681.1:p.Ile209Thr
|
|
NM_000108.5:c.770T>C
MANE Select
|
NP_000099.2:p.Ile257Thr
|
|