ENST00000696170.1:c.*163C=
|
ENSP00000512461.1:n.*163C=
|
|
ENST00000696171.1:c.558C=
|
ENSP00000512462.1:p.Gly186=
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|
ENST00000696172.1:c.338-2834C=
|
ENSP00000512463.1:n.338-2834C=
|
|
ENST00000378588.5:c.654C=
MANE Select
|
ENSP00000367851.4:p.Gly218=
|
|
ENST00000378588.4:c.654C=
|
ENSP00000367851.4:p.Gly218=
|
|
ENST00000465127.1:c.171+370121C=
|
ENSP00000417050.1:n.171+370121C=
|
|
NM_000397.3:c.654C= , LRG_53t1:c.654C=
|
NP_000388.2:p.Gly218=
|
|
XM_011543890.1:c.348C=
|
XP_011542192.1:p.Gly116=
|
|
NM_000397.4:c.654C=
MANE Select
|
NP_000388.2:p.Gly218=
|
|