ENST00000559133.6:c.6037+161_6037+164delinsAAGC
|
ENSP00000453958.2:n.6037+161_6037+164delinsAAGC
|
|
ENST00000674301.2:c.6037+161_6037+164delinsAAGC
|
ENSP00000501333.2:n.6037+161_6037+164delinsAAGC
|
|
ENST00000684448.1:n.4872_4875delinsAAGC
|
|
|
ENST00000316623.10:c.6037+161_6037+164delinsAAGC
MANE Select
|
ENSP00000325527.5:n.6037+161_6037+164delinsAAGC
|
|
ENST00000674301.1:c.1036+161_1036+164delinsAAGC
|
ENSP00000501333.1:n.1036+161_1036+164delinsAAGC
|
|
ENST00000316623.9:c.6037+161_6037+164delinsAAGC
|
ENSP00000325527.5:n.6037+161_6037+164delinsAAGC
|
|
ENST00000537463.6:c.*1800+161_*1800+164delinsAAGC
|
ENSP00000440294.2:n.*1800+161_*1800+164delinsAAGC
|
|
ENST00000559133.5:c.1344+161_1344+164delinsAAGC
|
|
|
ENST00000560820.1:n.157+161_157+164delinsAAGC
|
|
|
NM_000138.4:c.6037+161_6037+164delinsAAGC , LRG_778t1:c.6037+161_6037+164delinsAAGC
|
NP_000129.3:n.6037+161_6037+164delinsAAGC
|
|
NM_000138.5:c.6037+161_6037+164delinsAAGC
MANE Select
|
NP_000129.3:n.6037+161_6037+164delinsAAGC
|
|