ENST00000266771.10:c.842+416G>T
MANE Select
|
ENSP00000266771.5:n.842+416G>T
|
|
ENST00000266771.9:c.842+416G>T
|
ENSP00000266771.5:n.842+416G>T
|
|
ENST00000366292.6:n.1154+416G>T
|
|
|
ENST00000376740.8:c.421+416G>T
|
|
|
ENST00000376744.8:c.678+416G>T
|
|
|
ENST00000539703.1:n.492+416G>T
|
|
|
ENST00000614634.1:c.-1+416G>T
|
ENSP00000483143.1:n.-1+416G>T
|
|
NM_145648.3:c.842+416G>T
|
NP_663623.1:n.842+416G>T
|
|
XM_011537895.1:c.992+416G>T
|
XP_011536197.1:n.992+416G>T
|
|
XR_429081.2:n.865+416G>T
|
|
|
XR_944494.1:n.1015+416G>T
|
|
|
XR_944495.1:n.1015+416G>T
|
|
|
XR_944496.1:n.1015+416G>T
|
|
|
XR_944497.1:n.1015+416G>T
|
|
|
XM_017018791.1:c.992+416G>T
|
XP_016874280.1:n.992+416G>T
|
|
XM_017018792.1:c.992+416G>T
|
XP_016874281.1:n.992+416G>T
|
|
XM_017018793.1:c.842+416G>T
|
XP_016874282.1:n.842+416G>T
|
|
XR_002957287.1:n.865+416G>T
|
|
|
XR_944496.2:n.1015+416G>T
|
|
|
NM_145648.4:c.842+416G>T
MANE Select
|
NP_663623.1:n.842+416G>T
|
|