ENST00000696170.1:c.*116G=
|
ENSP00000512461.1:n.*116G=
|
|
ENST00000696171.1:c.511G=
|
ENSP00000512462.1:p.Glu171=
|
|
ENST00000696172.1:c.338-2881G=
|
ENSP00000512463.1:n.338-2881G=
|
|
ENST00000378588.5:c.607G=
MANE Select
|
ENSP00000367851.4:p.Glu203=
|
|
ENST00000378588.4:c.607G=
|
ENSP00000367851.4:p.Glu203=
|
|
ENST00000465127.1:c.171+370074G=
|
ENSP00000417050.1:n.171+370074G=
|
|
NM_000397.3:c.607G= , LRG_53t1:c.607G=
|
NP_000388.2:p.Glu203=
|
|
XM_011543890.1:c.301G=
|
XP_011542192.1:p.Glu101=
|
|
NM_000397.4:c.607G=
MANE Select
|
NP_000388.2:p.Glu203=
|
|