ENST00000696142.1:c.*178G=
|
ENSP00000512434.1:n.*178G=
|
|
ENST00000696143.1:c.637G=
|
ENSP00000512435.1:n.637G=
|
|
ENST00000696153.1:c.612G=
|
ENSP00000512444.1:p.Arg204=
|
|
ENST00000256474.3:c.501G=
MANE Select
|
ENSP00000256474.3:p.Arg167=
|
|
ENST00000256474.2:c.501G=
|
ENSP00000256474.2:p.Arg167=
|
|
ENST00000345392.2:c.378G=
|
ENSP00000344757.2:p.Arg126=
|
|
ENST00000477538.1:n.637G=
|
|
|
NM_000551.3:c.501G= , LRG_322t1:c.501G=
|
NP_000542.1:p.Arg167=
|
|
NM_198156.2:c.378G=
|
NP_937799.1:p.Arg126=
|
|
NM_001354723.1:c.*55G=
|
NP_001341652.1:n.*55G=
|
|
NM_000551.4:c.501G=
MANE Select
|
NP_000542.1:p.Arg167=
|
|
NM_001354723.2:c.*55G=
|
NP_001341652.1:n.*55G=
|
|
NM_198156.3:c.378G=
|
NP_937799.1:p.Arg126=
|
|