ENST00000559133.6:c.4188_4189delinsAG
|
ENSP00000453958.2:p.Thr1396=
|
|
ENST00000674301.2:c.4188_4189delinsAG
|
ENSP00000501333.2:p.Thr1396=
|
|
ENST00000684448.1:n.2862_2863delinsAG
|
|
|
ENST00000316623.10:c.4188_4189delinsAG
MANE Select
|
ENSP00000325527.5:p.Thr1396=
|
|
ENST00000316623.9:c.4188_4189delinsAG
|
ENSP00000325527.5:p.Thr1396=
|
|
ENST00000537463.6:c.860_861delinsAG
|
ENSP00000440294.2:p.Gln287=
|
|
NM_000138.4:c.4188_4189delinsAG , LRG_778t1:c.4188_4189delinsAG
|
NP_000129.3:p.Thr1396=
|
|
NM_000138.5:c.4188_4189delinsAG
MANE Select
|
NP_000129.3:p.Thr1396=
|
|