ENST00000474381.2:n.2965C=
|
|
|
ENST00000481849.6:n.2484C=
|
|
|
ENST00000497377.6:n.2391C=
|
|
|
ENST00000640094.2:c.895+116C=
|
ENSP00000491275.2:n.895+116C=
|
|
ENST00000696558.1:c.987C=
|
ENSP00000512716.1:n.987C=
|
|
ENST00000696559.1:c.918C=
|
ENSP00000512717.1:p.Val306=
|
|
ENST00000696560.1:c.918C=
|
ENSP00000512718.1:p.Val306=
|
|
ENST00000696561.1:c.918C=
|
ENSP00000512719.1:p.Val306=
|
|
ENST00000696562.1:c.918C=
|
ENSP00000512720.1:p.Val306=
|
|
ENST00000412585.7:c.918C=
MANE Select
|
ENSP00000399168.2:p.Val306=
|
|
ENST00000640094.1:c.88+116C=
|
ENSP00000491275.1:n.88+116C=
|
|
ENST00000412585.6:c.918C=
|
ENSP00000399168.2:p.Val306=
|
|
ENST00000463574.1:n.509C=
|
|
|
NM_005514.6:c.918C=
|
NP_005505.2:p.Val306=
|
|
XM_011514556.1:c.951C=
|
XP_011512858.1:p.Val317=
|
|
XM_011514557.1:c.895+116C=
|
XP_011512859.1:n.895+116C=
|
|
XR_926175.1:n.1357C=
|
|
|
NM_005514.7:c.918C=
|
NP_005505.2:p.Val306=
|
|
NM_005514.8:c.918C=
MANE Select
|
NP_005505.2:p.Val306=
|
|