|
NM_000124.4:c.*2155T>C
MANE Select
|
NP_000115.1:n.*2155T>C
|
|
ENST00000355832.10:c.*2155T>C
MANE Select
|
ENSP00000348089.5:n.*2155T>C
|
|
NM_000124.3:c.*2155T>C
|
NP_000115.1:n.*2155T>C
|
|
NM_001346440.1:c.*2155T>C
|
NP_001333369.1:n.*2155T>C
|
|
NM_001346440.2:c.*2155T>C
|
NP_001333369.1:n.*2155T>C
|
|
ENST00000355832.9:c.*2155T>C
|
ENSP00000348089.5:n.*2155T>C
|
|
ENST00000623073.3:c.*4933T>C
|
ENSP00000485650.1:n.*4933T>C
|
|
ENST00000624341.3:c.4469T>C
|
|
|
ENST00000679552.1:n.4846T>C
|
|
|
ENST00000679871.1:n.3783T>C
|
|
|
ENST00000679974.1:n.3686T>C
|
|
|
ENST00000681632.1:n.8040T>C
|
|
|
ENST00000681659.1:c.*2155T>C
|
ENSP00000505631.1:n.*2155T>C
|
|
XR_945953.1:n.243-14905A>G
|
|