ENST00000474381.2:n.3113T>G
|
|
|
ENST00000481849.6:n.3073T>G
|
|
|
ENST00000497377.6:n.2980T>G
|
|
|
ENST00000640094.2:c.949T>G
|
ENSP00000491275.2:p.Ser317Ala
|
|
ENST00000696558.1:c.1135T>G
|
ENSP00000512716.1:n.1135T>G
|
|
ENST00000696559.1:c.1066T>G
|
ENSP00000512717.1:p.Ser356Ala
|
|
ENST00000696560.1:c.1066T>G
|
ENSP00000512718.1:p.Ser356Ala
|
|
ENST00000696561.1:c.1066T>G
|
ENSP00000512719.1:p.Ser356Ala
|
|
ENST00000696562.1:c.1066T>G
|
ENSP00000512720.1:p.Ser356Ala
|
|
ENST00000412585.7:c.1066T>G
MANE Select
|
ENSP00000399168.2:p.Ser356Ala
|
|
ENST00000640094.1:c.142T>G
|
ENSP00000491275.1:p.Ser48Ala
|
|
ENST00000412585.6:c.1066T>G
|
ENSP00000399168.2:p.Ser356Ala
|
|
ENST00000481849.5:n.301T>G
|
|
|
ENST00000497377.5:n.465T>G
|
|
|
NM_005514.6:c.1066T>G
|
NP_005505.2:p.Ser356Ala
|
|
XM_011514556.1:c.1099T>G
|
XP_011512858.1:p.Ser367Ala
|
|
XM_011514557.1:c.949T>G
|
XP_011512859.1:p.Ser317Ala
|
|
XR_926175.1:n.1505T>G
|
|
|
NM_005514.7:c.1066T>G
|
NP_005505.2:p.Ser356Ala
|
|
NM_005514.8:c.1066T>G
MANE Select
|
NP_005505.2:p.Ser356Ala
|
|