ENST00000703783.1:n.260T>C
|
|
|
ENST00000703785.1:n.341T>C
|
|
|
ENST00000262464.9:c.3476T>C
MANE Select
|
ENSP00000262464.4:p.Ile1159Thr
|
|
ENST00000262464.8:c.3476T>C
|
ENSP00000262464.4:p.Ile1159Thr
|
|
ENST00000507835.5:c.26T>C
|
ENSP00000426839.1:p.Ile9Thr
|
|
ENST00000508053.5:c.3476T>C
|
ENSP00000424571.1:p.Ile1159Thr
|
|
ENST00000508989.5:c.3377T>C
|
ENSP00000425596.1:p.Ile1126Thr
|
|
ENST00000619499.4:c.3473T>C
|
ENSP00000482132.1:p.Ile1158Thr
|
|
NM_001999.3:c.3476T>C
|
NP_001990.2:p.Ile1159Thr
|
|
XM_017009228.2:c.3323T>C
|
XP_016864717.1:p.Ile1108Thr
|
|
NM_001999.4:c.3476T>C
MANE Select
|
NP_001990.2:p.Ile1159Thr
|
|