ENST00000696156.1:c.*36C>G
|
ENSP00000512446.1:n.*36C>G
|
|
ENST00000696157.1:c.*841C>G
|
ENSP00000512447.1:n.*841C>G
|
|
ENST00000696158.1:c.*878C>G
|
ENSP00000512448.1:n.*878C>G
|
|
ENST00000696159.1:c.*547C>G
|
ENSP00000512449.1:n.*547C>G
|
|
ENST00000696160.1:c.*36C>G
|
ENSP00000512450.1:n.*36C>G
|
|
ENST00000696161.1:c.754C>G
|
ENSP00000512451.1:p.His252Asp
|
|
ENST00000696162.1:c.*1343C>G
|
ENSP00000512452.1:n.*1343C>G
|
|
ENST00000696163.1:c.*36C>G
|
ENSP00000512453.1:n.*36C>G
|
|
ENST00000261623.8:c.*36C>G
MANE Select
|
ENSP00000261623.3:n.*36C>G
|
|
ENST00000261623.7:c.*36C>G
|
ENSP00000261623.3:n.*36C>G
|
|
NM_000101.3:c.*36C>G
|
NP_000092.2:n.*36C>G
|
|
NM_000101.4:c.*36C>G
MANE Select
|
NP_000092.2:n.*36C>G
|
|