ENST00000696170.1:c.*162G>C
|
ENSP00000512461.1:n.*162G>C
|
|
ENST00000696171.1:c.557G>C
|
ENSP00000512462.1:p.Gly186Ala
|
|
ENST00000696172.1:c.338-2835G>C
|
ENSP00000512463.1:n.338-2835G>C
|
|
ENST00000378588.5:c.653G>C
MANE Select
|
ENSP00000367851.4:p.Gly218Ala
|
|
ENST00000378588.4:c.653G>C
|
ENSP00000367851.4:p.Gly218Ala
|
|
ENST00000465127.1:c.171+370120G>C
|
ENSP00000417050.1:n.171+370120G>C
|
|
NM_000397.3:c.653G>C , LRG_53t1:c.653G>C
|
NP_000388.2:p.Gly218Ala
|
|
XM_011543890.1:c.347G>C
|
XP_011542192.1:p.Gly116Ala
|
|
NM_000397.4:c.653G>C
MANE Select
|
NP_000388.2:p.Gly218Ala
|
|