ENST00000266771.10:c.761G>T
MANE Select
|
ENSP00000266771.5:p.Gly254Val
|
|
ENST00000266771.9:c.761G>T
|
ENSP00000266771.5:p.Gly254Val
|
|
ENST00000366292.6:n.1073G>T
|
|
|
ENST00000376740.8:c.340G>T
|
|
|
ENST00000376744.8:c.597G>T
|
|
|
ENST00000539703.1:n.411G>T
|
|
|
ENST00000614634.1:c.-82G>T
|
ENSP00000483143.1:n.-82G>T
|
|
NM_145648.3:c.761G>T
|
NP_663623.1:p.Gly254Val
|
|
XM_011537895.1:c.911G>T
|
XP_011536197.1:p.Gly304Val
|
|
XR_429081.2:n.784G>T
|
|
|
XR_944494.1:n.934G>T
|
|
|
XR_944495.1:n.934G>T
|
|
|
XR_944496.1:n.934G>T
|
|
|
XR_944497.1:n.934G>T
|
|
|
XM_017018791.1:c.911G>T
|
XP_016874280.1:p.Gly304Val
|
|
XM_017018792.1:c.911G>T
|
XP_016874281.1:p.Gly304Val
|
|
XM_017018793.1:c.761G>T
|
XP_016874282.1:p.Gly254Val
|
|
XR_002957287.1:n.784G>T
|
|
|
XR_944496.2:n.934G>T
|
|
|
NM_145648.4:c.761G>T
MANE Select
|
NP_663623.1:p.Gly254Val
|
|