ENST00000696142.1:c.*211G>A
|
ENSP00000512434.1:n.*211G>A
|
|
ENST00000696143.1:c.670G>A
|
ENSP00000512435.1:n.670G>A
|
|
ENST00000696153.1:c.645G>A
|
ENSP00000512444.1:p.Leu215=
|
|
ENST00000256474.3:c.534G>A
MANE Select
|
ENSP00000256474.3:p.Leu178=
|
|
ENST00000256474.2:c.534G>A
|
ENSP00000256474.2:p.Leu178=
|
|
ENST00000345392.2:c.411G>A
|
ENSP00000344757.2:p.Leu137=
|
|
ENST00000477538.1:n.670G>A
|
|
|
NM_000551.3:c.534G>A , LRG_322t1:c.534G>A
|
NP_000542.1:p.Leu178=
|
|
NM_198156.2:c.411G>A
|
NP_937799.1:p.Leu137=
|
|
NM_001354723.1:c.*88G>A
|
NP_001341652.1:n.*88G>A
|
|
NM_000551.4:c.534G>A
MANE Select
|
NP_000542.1:p.Leu178=
|
|
NM_001354723.2:c.*88G>A
|
NP_001341652.1:n.*88G>A
|
|
NM_198156.3:c.411G>A
|
NP_937799.1:p.Leu137=
|
|