|
ENST00000264956.11:c.2164C>T
(EVC)
MANE Select
|
ENSP00000264956.6:p.Gln722Ter
|
|
|
ENST00000264956.10:c.2164C>T
(EVC)
|
ENSP00000264956.6:p.Gln722Ter
|
|
|
ENST00000506216.5:n.1647+26842G>A
(CRMP1)
|
|
|
|
ENST00000515113.1:n.388C>T
(EVC)
|
|
|
|
NM_001306090.1:c.2164C>T
(EVC)
|
NP_001293019.1:p.Gln722Ter
|
|
|
NM_153717.2:c.2164C>T
(EVC)
|
NP_714928.1:p.Gln722Ter
|
|
|
XM_006713865.2:c.2164C>T
(EVC)
|
XP_006713928.1:p.Gln722Ter
|
|
|
XM_006713866.2:c.2164C>T
(EVC)
|
XP_006713929.1:p.Gln722Ter
|
|
|
XR_427473.2:n.2354C>T
(EVC)
|
|
|
|
XR_427475.2:n.2354C>T
(EVC)
|
|
|
|
XR_427476.2:n.2354C>T
(EVC)
|
|
|
|
XR_924920.1:n.2354C>T
(EVC)
|
|
|
|
XR_924921.1:n.2354C>T
(EVC)
|
|
|
|
XR_924922.1:n.2354C>T
(EVC)
|
|
|
|
XR_924923.1:n.2354C>T
(EVC)
|
|
|
|
XR_924924.1:n.2354C>T
(EVC)
|
|
|
|
XR_924925.1:n.2354C>T
(EVC)
|
|
|
|
XR_924926.1:n.2354C>T
(EVC)
|
|
|
|
XR_924927.1:n.2354C>T
(EVC)
|
|
|
|
XR_924928.1:n.2356C>T
(EVC)
|
|
|
|
XM_006713865.3:c.2164C>T
(EVC)
|
XP_006713928.1:p.Gln722Ter
|
|
|
XM_006713866.3:c.2164C>T
(EVC)
|
XP_006713929.1:p.Gln722Ter
|
|
|
XR_001741164.1:n.2344C>T
(EVC)
|
|
|
|
XR_001741165.1:n.2344C>T
(EVC)
|
|
|
|
XR_001741166.1:n.2344C>T
(EVC)
|
|
|
|
XR_001741167.1:n.2344C>T
(EVC)
|
|
|
|
XR_001741168.1:n.2344C>T
(EVC)
|
|
|
|
XR_001741169.2:n.2208C>T
(EVC)
|
|
|
|
XR_001741170.1:n.2346C>T
(EVC)
|
|
|
|
XR_001741171.1:n.1649C>T
(EVC)
|
|
|
|
XR_427473.3:n.2344C>T
(EVC)
|
|
|
|
XR_427475.3:n.2344C>T
(EVC)
|
|
|
|
XR_427476.3:n.2344C>T
(EVC)
|
|
|
|
XR_924920.2:n.2344C>T
(EVC)
|
|
|
|
XR_924921.2:n.2344C>T
(EVC)
|
|
|
|
XR_924922.2:n.2344C>T
(EVC)
|
|
|
|
XR_924924.2:n.2344C>T
(EVC)
|
|
|
|
XR_924925.2:n.2344C>T
(EVC)
|
|
|
|
XR_924926.2:n.2344C>T
(EVC)
|
|
|
|
NM_153717.3:c.2164C>T
(EVC)
MANE Select
|
NP_714928.1:p.Gln722Ter
|
|
|
NM_001306090.2:c.2164C>T
(EVC)
|
NP_001293019.1:p.Gln722Ter
|
|
