ENST00000559133.6:c.*1686_*1687insTG
|
ENSP00000453958.2:n.*1686_*1687insTG
|
|
ENST00000682158.1:n.2259_2260insTG
|
|
|
ENST00000682170.1:n.3059_3060insTG
|
|
|
ENST00000682767.1:n.2175_2176insTG
|
|
|
ENST00000316623.10:c.*262_*263insTG
MANE Select
|
ENSP00000325527.5:n.*262_*263insTG
|
|
ENST00000316623.9:c.*262_*263insTG
|
ENSP00000325527.5:n.*262_*263insTG
|
|
ENST00000559133.5:c.4247_4248insTG
|
|
|
NM_000138.4:c.*262_*263insTG , LRG_778t1:c.*262_*263insTG
|
NP_000129.3:n.*262_*263insTG
|
|
NM_000138.5:c.*262_*263insTG
MANE Select
|
NP_000129.3:n.*262_*263insTG
|
|