ENST00000408957.7:c.*1787_*1799delinsAAAAAAAAAAAAG
(TIGD1)
MANE Select
|
ENSP00000386186.3:n.*1787_*1799delinsAAAAAAAAAAAAG
|
|
ENST00000651502.1:c.*592_*604delinsCTTTTTTTTTTTT
(CHRNG)
MANE Select
|
ENSP00000498757.1:n.*592_*604delinsCTTTTTTTTTTTT
|
|
ENST00000389494.7:c.*592_*604delinsCTTTTTTTTTTTT
(CHRNG)
|
ENSP00000374145.3:n.*592_*604delinsCTTTTTTTTTTTT
|
|
NM_005199.4:c.*592_*604delinsCTTTTTTTTTTTT
(CHRNG)
|
NP_005190.4:n.*592_*604delinsCTTTTTTTTTTTT
|
|
NM_005199.5:c.*592_*604delinsCTTTTTTTTTTTT
(CHRNG)
MANE Select
|
NP_005190.4:n.*592_*604delinsCTTTTTTTTTTTT
|
|
NM_145702.4:c.*1787_*1799delinsAAAAAAAAAAAAG
(TIGD1)
MANE Select
|
NP_663748.1:n.*1787_*1799delinsAAAAAAAAAAAAG
|
|