ENST00000706625.1:c.58A=
|
ENSP00000516471.1:p.Lys20=
|
|
ENST00000376033.3:c.42A=
MANE Select
|
ENSP00000365201.2:p.Gly14=
|
|
ENST00000376007.8:c.42A=
|
ENSP00000365175.4:p.Gly14=
|
|
ENST00000376033.2:c.42A=
|
ENSP00000365201.2:p.Gly14=
|
|
ENST00000469577.5:n.136-1430A=
|
|
|
NM_004638.3:c.42A=
|
NP_004629.3:p.Gly14=
|
|
NM_080686.2:c.42A=
|
NP_542417.2:p.Gly14=
|
|
XM_011514890.1:c.42A=
|
XP_011513192.1:p.Gly14=
|
|
XM_017011274.1:c.42A=
|
XP_016866763.1:p.Gly14=
|
|
NM_004638.4:c.42A=
MANE Select
|
NP_004629.3:p.Gly14=
|
|
NM_080686.3:c.42A=
|
NP_542417.2:p.Gly14=
|
|