ENST00000369733.8:c.743C>T
|
ENSP00000358748.3:p.Thr248Ile
|
|
ENST00000648076.2:c.743C>T
MANE Select
|
ENSP00000497653.1:p.Thr248Ile
|
|
ENST00000649118.1:n.858C>T
|
|
|
ENST00000650263.1:c.695C>T
|
ENSP00000497850.1:p.Thr232Ile
|
|
ENST00000353479.9:c.743C>T
|
ENSP00000340937.5:p.Thr248Ile
|
|
ENST00000369733.7:c.743C>T
|
ENSP00000358748.3:p.Thr248Ile
|
|
ENST00000393211.3:c.743C>T
|
ENSP00000376905.3:p.Thr248Ile
|
|
ENST00000488320.1:n.88C>T
|
|
|
NM_000494.3:c.743C>T
|
NP_000485.3:p.Thr248Ile
|
|
NM_000494.4:c.743C>T
MANE Select
|
NP_000485.3:p.Thr248Ile
|
|