ENST00000507079.6:c.-395G=
|
ENSP00000426147.2:n.-395G=
|
|
ENST00000226574.9:c.-349G=
MANE Select
|
ENSP00000226574.4:n.-349G=
|
|
ENST00000652619.1:c.-395G=
|
ENSP00000499031.1:n.-395G=
|
|
ENST00000226574.8:c.-349G=
|
ENSP00000226574.4:n.-349G=
|
|
ENST00000394820.8:c.-349G=
|
ENSP00000378297.4:n.-349G=
|
|
NM_001165412.1:c.-349G=
|
NP_001158884.1:n.-349G=
|
|
NM_003998.3:c.-349G=
|
NP_003989.2:n.-349G=
|
|
XM_011532467.1:c.445C=
|
XP_011530769.1:p.Arg149=
|
|
NR_136202.1:n.48+992C=
|
|
|
XM_024454067.1:c.-395G=
|
XP_024309835.1:n.-395G=
|
|
XM_024454069.1:c.-395G=
|
XP_024309837.1:n.-395G=
|
|
NM_003998.4:c.-349G=
MANE Select
|
NP_003989.2:n.-349G=
|
|
NM_001165412.2:c.-349G=
|
NP_001158884.1:n.-349G=
|
|
NM_001382626.1:c.-419G=
|
NP_001369555.1:n.-419G=
|
|
NM_001382627.1:c.-419G=
|
NP_001369556.1:n.-419G=
|
|
NM_001382628.1:c.-342G=
|
NP_001369557.1:n.-342G=
|
|