ENST00000696142.1:c.*210T=
|
ENSP00000512434.1:n.*210T=
|
|
ENST00000696143.1:c.669T=
|
ENSP00000512435.1:n.669T=
|
|
ENST00000696153.1:c.644T=
|
ENSP00000512444.1:p.Leu215=
|
|
ENST00000256474.3:c.533T=
MANE Select
|
ENSP00000256474.3:p.Leu178=
|
|
ENST00000256474.2:c.533T=
|
ENSP00000256474.2:p.Leu178=
|
|
ENST00000345392.2:c.410T=
|
ENSP00000344757.2:p.Leu137=
|
|
ENST00000477538.1:n.669T=
|
|
|
NM_000551.3:c.533T= , LRG_322t1:c.533T=
|
NP_000542.1:p.Leu178=
|
|
NM_198156.2:c.410T=
|
NP_937799.1:p.Leu137=
|
|
NM_001354723.1:c.*87T=
|
NP_001341652.1:n.*87T=
|
|
NM_000551.4:c.533T=
MANE Select
|
NP_000542.1:p.Leu178=
|
|
NM_001354723.2:c.*87T=
|
NP_001341652.1:n.*87T=
|
|
NM_198156.3:c.410T=
|
NP_937799.1:p.Leu137=
|
|