ENST00000474381.2:n.2496T>C
|
|
|
ENST00000481849.6:n.2093-171T>C
|
|
|
ENST00000497377.6:n.2093-171T>C
|
|
|
ENST00000640094.2:c.620-171T>C
|
ENSP00000491275.2:n.620-171T>C
|
|
ENST00000696558.1:c.663T>C
|
ENSP00000512716.1:p.Leu221=
|
|
ENST00000696559.1:c.620-171T>C
|
ENSP00000512717.1:n.620-171T>C
|
|
ENST00000696560.1:c.620-171T>C
|
ENSP00000512718.1:n.620-171T>C
|
|
ENST00000696561.1:c.620-171T>C
|
ENSP00000512719.1:n.620-171T>C
|
|
ENST00000696562.1:c.620-171T>C
|
ENSP00000512720.1:n.620-171T>C
|
|
ENST00000412585.7:c.620-171T>C
MANE Select
|
ENSP00000399168.2:n.620-171T>C
|
|
ENST00000412585.6:c.620-171T>C
|
ENSP00000399168.2:n.620-171T>C
|
|
ENST00000434333.1:c.653-171T>C
|
ENSP00000405931.1:n.653-171T>C
|
|
ENST00000463574.1:n.40T>C
|
|
|
ENST00000474381.1:n.898T>C
|
|
|
ENST00000498007.1:n.886-171T>C
|
|
|
NM_005514.6:c.620-171T>C
|
NP_005505.2:n.620-171T>C
|
|
XM_011514556.1:c.653-171T>C
|
XP_011512858.1:n.653-171T>C
|
|
XM_011514557.1:c.620-171T>C
|
XP_011512859.1:n.620-171T>C
|
|
XR_926175.1:n.1033T>C
|
|
|
NM_005514.7:c.620-171T>C
|
NP_005505.2:n.620-171T>C
|
|
NM_005514.8:c.620-171T>C
MANE Select
|
NP_005505.2:n.620-171T>C
|
|