ENST00000355832.10:c.3959T>C
MANE Select
|
ENSP00000348089.5:p.Ile1320Thr
|
|
ENST00000679552.1:n.1030T>C
|
|
|
ENST00000679871.1:n.1105T>C
|
|
|
ENST00000679974.1:n.1008T>C
|
|
|
ENST00000681632.1:n.5362T>C
|
|
|
ENST00000681659.1:c.3800T>C
|
ENSP00000505631.1:p.Ile1267Thr
|
|
ENST00000355832.9:c.3959T>C
|
ENSP00000348089.5:p.Ile1320Thr
|
|
ENST00000465653.1:n.281T>C
|
|
|
ENST00000623073.3:c.*2255T>C
|
ENSP00000485650.1:n.*2255T>C
|
|
ENST00000623115.3:c.2069T>C
|
ENSP00000485321.1:p.Ile690Thr
|
|
ENST00000624341.3:c.1791T>C
|
|
|
NM_000124.3:c.3959T>C
|
NP_000115.1:p.Ile1320Thr
|
|
XR_945953.1:n.243-10189A>G
|
|
|
NM_001346440.1:c.3959T>C
|
NP_001333369.1:p.Ile1320Thr
|
|
NM_000124.4:c.3959T>C
MANE Select
|
NP_000115.1:p.Ile1320Thr
|
|
NM_001346440.2:c.3959T>C
|
NP_001333369.1:p.Ile1320Thr
|
|