ENST00000703783.1:n.944T>C
|
|
|
ENST00000703785.1:n.1025T>C
|
|
|
ENST00000262464.9:c.4160T>C
MANE Select
|
ENSP00000262464.4:p.Ile1387Thr
|
|
ENST00000262464.8:c.4160T>C
|
ENSP00000262464.4:p.Ile1387Thr
|
|
ENST00000507835.5:c.710T>C
|
ENSP00000426839.1:p.Ile237Thr
|
|
ENST00000508053.5:c.4160T>C
|
ENSP00000424571.1:p.Ile1387Thr
|
|
ENST00000508989.5:c.4061T>C
|
ENSP00000425596.1:p.Ile1354Thr
|
|
ENST00000619499.4:c.4157T>C
|
ENSP00000482132.1:p.Ile1386Thr
|
|
NM_001999.3:c.4160T>C
|
NP_001990.2:p.Ile1387Thr
|
|
XM_017009228.2:c.4007T>C
|
XP_016864717.1:p.Ile1336Thr
|
|
NM_001999.4:c.4160T>C
MANE Select
|
NP_001990.2:p.Ile1387Thr
|
|