ENST00000559133.6:c.5917+215_5917+231delinsATATGTATATATATATG
|
ENSP00000453958.2:n.5917+215_5917+231delinsATATGTATATATATATG
|
|
ENST00000674301.2:c.5917+215_5917+231delinsATATGTATATATATATG
|
ENSP00000501333.2:n.5917+215_5917+231delinsATATGTATATATATATG
|
|
ENST00000684448.1:n.4591+215_4591+231delinsATATGTATATATATATG
|
|
|
ENST00000316623.10:c.5917+215_5917+231delinsATATGTATATATATATG
MANE Select
|
ENSP00000325527.5:n.5917+215_5917+231delinsATATGTATATATATATG
|
|
ENST00000674301.1:c.916+215_916+231delinsATATGTATATATATATG
|
ENSP00000501333.1:n.916+215_916+231delinsATATGTATATATATATG
|
|
ENST00000316623.9:c.5917+215_5917+231delinsATATGTATATATATATG
|
ENSP00000325527.5:n.5917+215_5917+231delinsATATGTATATATATATG
|
|
ENST00000537463.6:c.*1680+215_*1680+231delinsATATGTATATATATATG
|
ENSP00000440294.2:n.*1680+215_*1680+231delinsATATGTATATATATAT...
|
|
ENST00000559133.5:c.1224+215_1224+231delinsATATGTATATATATATG
|
|
|
ENST00000560820.1:n.37+215_37+231delinsATATGTATATATATATG
|
|
|
NM_000138.4:c.5917+215_5917+231delinsATATGTATATATATATG , LRG_778t1:c.5917+215_5917+231delinsATATGTATATATATATG
|
NP_000129.3:n.5917+215_5917+231delinsATATGTATATATATATG
|
|
NM_000138.5:c.5917+215_5917+231delinsATATGTATATATATATG
MANE Select
|
NP_000129.3:n.5917+215_5917+231delinsATATGTATATATATATG
|
|