ENST00000223051.8:c.*217T>C
MANE Select
|
ENSP00000223051.3:n.*217T>C
|
|
ENST00000223051.7:c.*217T>C
|
ENSP00000223051.3:n.*217T>C
|
|
ENST00000431692.5:c.*1298T>C
|
ENSP00000413905.1:n.*1298T>C
|
|
ENST00000462090.5:n.1659T>C
|
|
|
ENST00000462107.1:c.*217T>C
|
ENSP00000420525.1:n.*217T>C
|
|
ENST00000465294.5:n.2543T>C
|
|
|
ENST00000476304.5:n.2244T>C
|
|
|
ENST00000490084.5:c.1976T>C
|
|
|
NM_001206855.1:c.*217T>C
|
NP_001193784.1:n.*217T>C
|
|
NM_003227.3:c.*217T>C
|
NP_003218.2:n.*217T>C
|
|
XM_005250553.3:c.*217T>C
|
XP_005250610.1:n.*217T>C
|
|
NM_001206855.2:c.*217T>C
|
NP_001193784.1:n.*217T>C
|
|
XM_005250553.4:c.*217T>C
|
XP_005250610.1:n.*217T>C
|
|
XM_017012573.1:c.*217T>C
|
XP_016868062.1:n.*217T>C
|
|
NM_003227.4:c.*217T>C
MANE Select
|
NP_003218.2:n.*217T>C
|
|
NM_001206855.3:c.*217T>C
|
NP_001193784.1:n.*217T>C
|
|