ENST00000408957.7:c.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA
(TIGD1)
MANE Select
|
ENSP00000386186.3:n.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA
|
|
ENST00000651502.1:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
(CHRNG)
MANE Select
|
ENSP00000498757.1:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
|
|
ENST00000389494.7:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
(CHRNG)
|
ENSP00000374145.3:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
|
|
NM_005199.5:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
(CHRNG)
MANE Select
|
NP_005190.4:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
|
|
NM_145702.4:c.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA
(TIGD1)
MANE Select
|
NP_663748.1:n.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA
|
|