ENST00000696142.1:c.*145T>G
|
ENSP00000512434.1:n.*145T>G
|
|
ENST00000696143.1:c.604T>G
|
ENSP00000512435.1:n.604T>G
|
|
ENST00000696153.1:c.579T>G
|
ENSP00000512444.1:p.Tyr193Ter
|
|
ENST00000256474.3:c.468T>G
MANE Select
|
ENSP00000256474.3:p.Tyr156Ter
|
|
ENST00000256474.2:c.468T>G
|
ENSP00000256474.2:p.Tyr156Ter
|
|
ENST00000345392.2:c.345T>G
|
ENSP00000344757.2:p.Tyr115Ter
|
|
ENST00000477538.1:n.604T>G
|
|
|
NM_000551.3:c.468T>G , LRG_322t1:c.468T>G
|
NP_000542.1:p.Tyr156Ter
|
|
NM_198156.2:c.345T>G
|
NP_937799.1:p.Tyr115Ter
|
|
NM_001354723.1:c.*22T>G
|
NP_001341652.1:n.*22T>G
|
|
NM_000551.4:c.468T>G
MANE Select
|
NP_000542.1:p.Tyr156Ter
|
|
NM_001354723.2:c.*22T>G
|
NP_001341652.1:n.*22T>G
|
|
NM_198156.3:c.345T>G
|
NP_937799.1:p.Tyr115Ter
|
|