ENST00000696142.1:c.*203A>G
|
ENSP00000512434.1:n.*203A>G
|
|
ENST00000696143.1:c.662A>G
|
ENSP00000512435.1:n.662A>G
|
|
ENST00000696153.1:c.637A>G
|
ENSP00000512444.1:p.Arg213Gly
|
|
ENST00000256474.3:c.526A>G
MANE Select
|
ENSP00000256474.3:p.Arg176Gly
|
|
ENST00000256474.2:c.526A>G
|
ENSP00000256474.2:p.Arg176Gly
|
|
ENST00000345392.2:c.403A>G
|
ENSP00000344757.2:p.Arg135Gly
|
|
ENST00000477538.1:n.662A>G
|
|
|
NM_000551.3:c.526A>G , LRG_322t1:c.526A>G
|
NP_000542.1:p.Arg176Gly
|
|
NM_198156.2:c.403A>G
|
NP_937799.1:p.Arg135Gly
|
|
NM_001354723.1:c.*80A>G
|
NP_001341652.1:n.*80A>G
|
|
NM_000551.4:c.526A>G
MANE Select
|
NP_000542.1:p.Arg176Gly
|
|
NM_001354723.2:c.*80A>G
|
NP_001341652.1:n.*80A>G
|
|
NM_198156.3:c.403A>G
|
NP_937799.1:p.Arg135Gly
|
|