ENST00000696170.1:c.*574C>G
|
ENSP00000512461.1:n.*574C>G
|
|
ENST00000696171.1:c.969C>G
|
ENSP00000512462.1:p.Ile323Met
|
|
ENST00000378588.5:c.1065C>G
MANE Select
|
ENSP00000367851.4:p.Ile355Met
|
|
ENST00000378588.4:c.1065C>G
|
ENSP00000367851.4:p.Ile355Met
|
|
ENST00000465127.1:c.171+378044C>G
|
ENSP00000417050.1:n.171+378044C>G
|
|
ENST00000492288.1:n.490C>G
|
|
|
NM_000397.3:c.1065C>G , LRG_53t1:c.1065C>G
|
NP_000388.2:p.Ile355Met
|
|
XM_011543890.1:c.759C>G
|
XP_011542192.1:p.Ile253Met
|
|
NM_000397.4:c.1065C>G
MANE Select
|
NP_000388.2:p.Ile355Met
|
|