ENST00000311907.10:c.716G>T
MANE Select
|
ENSP00000308541.5:p.Ser239Ile
|
|
ENST00000311907.9:c.716G>T
|
ENSP00000308541.5:p.Ser239Ile
|
|
ENST00000442468.1:c.686G>T
|
ENSP00000387413.1:p.Ser229Ile
|
|
ENST00000490274.1:n.496G>T
|
|
|
ENST00000530231.5:c.716G>T
|
ENSP00000433907.1:p.Ser239Ile
|
|
NM_000506.3:c.716G>T
|
NP_000497.1:p.Ser239Ile
|
|
NM_000506.4:c.716G>T , LRG_551t1:c.716G>T
|
NP_000497.1:p.Ser239Ile
|
|
NM_001311257.1:c.668G>T
|
NP_001298186.1:p.Ser223Ile
|
|
XR_428840.2:n.760G>T
|
|
|
XR_428840.4:n.751G>T
|
|
|
NM_000506.5:c.716G>T
MANE Select
|
NP_000497.1:p.Ser239Ile
|
|
NM_001311257.2:c.668G>T
|
NP_001298186.1:p.Ser223Ile
|
|