ENST00000696170.1:c.*139T>G
|
ENSP00000512461.1:n.*139T>G
|
|
ENST00000696171.1:c.534T>G
|
ENSP00000512462.1:p.His178Gln
|
|
ENST00000696172.1:c.338-2858T>G
|
ENSP00000512463.1:n.338-2858T>G
|
|
ENST00000378588.5:c.630T>G
MANE Select
|
ENSP00000367851.4:p.His210Gln
|
|
ENST00000378588.4:c.630T>G
|
ENSP00000367851.4:p.His210Gln
|
|
ENST00000465127.1:c.171+370097T>G
|
ENSP00000417050.1:n.171+370097T>G
|
|
NM_000397.3:c.630T>G , LRG_53t1:c.630T>G
|
NP_000388.2:p.His210Gln
|
|
XM_011543890.1:c.324T>G
|
XP_011542192.1:p.His108Gln
|
|
NM_000397.4:c.630T>G
MANE Select
|
NP_000388.2:p.His210Gln
|
|