ENST00000696170.1:c.*164C>G
|
ENSP00000512461.1:n.*164C>G
|
|
ENST00000696171.1:c.559C>G
|
ENSP00000512462.1:p.Leu187Val
|
|
ENST00000696172.1:c.338-2833C>G
|
ENSP00000512463.1:n.338-2833C>G
|
|
ENST00000378588.5:c.655C>G
MANE Select
|
ENSP00000367851.4:p.Leu219Val
|
|
ENST00000378588.4:c.655C>G
|
ENSP00000367851.4:p.Leu219Val
|
|
ENST00000465127.1:c.171+370122C>G
|
ENSP00000417050.1:n.171+370122C>G
|
|
NM_000397.3:c.655C>G , LRG_53t1:c.655C>G
|
NP_000388.2:p.Leu219Val
|
|
XM_011543890.1:c.349C>G
|
XP_011542192.1:p.Leu117Val
|
|
NM_000397.4:c.655C>G
MANE Select
|
NP_000388.2:p.Leu219Val
|
|