ENST00000474381.2:n.2711G>C
|
|
|
ENST00000481849.6:n.2137G>C
|
|
|
ENST00000497377.6:n.2137G>C
|
|
|
ENST00000640094.2:c.664G>C
|
ENSP00000491275.2:p.Glu222Gln
|
|
ENST00000696558.1:c.733G>C
|
ENSP00000512716.1:n.733G>C
|
|
ENST00000696559.1:c.664G>C
|
ENSP00000512717.1:p.Glu222Gln
|
|
ENST00000696560.1:c.664G>C
|
ENSP00000512718.1:p.Glu222Gln
|
|
ENST00000696561.1:c.664G>C
|
ENSP00000512719.1:p.Glu222Gln
|
|
ENST00000696562.1:c.664G>C
|
ENSP00000512720.1:p.Glu222Gln
|
|
ENST00000412585.7:c.664G>C
MANE Select
|
ENSP00000399168.2:p.Glu222Gln
|
|
ENST00000412585.6:c.664G>C
|
ENSP00000399168.2:p.Glu222Gln
|
|
ENST00000434333.1:c.697G>C
|
ENSP00000405931.1:p.Glu233Gln
|
|
ENST00000463574.1:n.255G>C
|
|
|
ENST00000474381.1:n.1113G>C
|
|
|
ENST00000498007.1:n.930G>C
|
|
|
NM_005514.6:c.664G>C
|
NP_005505.2:p.Glu222Gln
|
|
XM_011514556.1:c.697G>C
|
XP_011512858.1:p.Glu233Gln
|
|
XM_011514557.1:c.664G>C
|
XP_011512859.1:p.Glu222Gln
|
|
XR_926175.1:n.1103G>C
|
|
|
NM_005514.7:c.664G>C
|
NP_005505.2:p.Glu222Gln
|
|
NM_005514.8:c.664G>C
MANE Select
|
NP_005505.2:p.Glu222Gln
|
|