ENST00000696156.1:c.*20T>G
|
ENSP00000512446.1:n.*20T>G
|
|
ENST00000696157.1:c.*825T>G
|
ENSP00000512447.1:n.*825T>G
|
|
ENST00000696158.1:c.*862T>G
|
ENSP00000512448.1:n.*862T>G
|
|
ENST00000696159.1:c.*531T>G
|
ENSP00000512449.1:n.*531T>G
|
|
ENST00000696160.1:c.*20T>G
|
ENSP00000512450.1:n.*20T>G
|
|
ENST00000696161.1:c.738T>G
|
ENSP00000512451.1:p.Pro246=
|
|
ENST00000696162.1:c.*1327T>G
|
ENSP00000512452.1:n.*1327T>G
|
|
ENST00000696163.1:c.*20T>G
|
ENSP00000512453.1:n.*20T>G
|
|
ENST00000261623.8:c.*20T>G
MANE Select
|
ENSP00000261623.3:n.*20T>G
|
|
ENST00000261623.7:c.*20T>G
|
ENSP00000261623.3:n.*20T>G
|
|
NM_000101.3:c.*20T>G
|
NP_000092.2:n.*20T>G
|
|
NM_000101.4:c.*20T>G
MANE Select
|
NP_000092.2:n.*20T>G
|
|