ENST00000696142.1:c.*230T=
|
ENSP00000512434.1:n.*230T=
|
|
ENST00000696143.1:c.689T=
|
ENSP00000512435.1:n.689T=
|
|
ENST00000696153.1:c.664T=
|
ENSP00000512444.1:p.Tyr222=
|
|
ENST00000256474.3:c.553T=
MANE Select
|
ENSP00000256474.3:p.Tyr185=
|
|
ENST00000256474.2:c.553T=
|
ENSP00000256474.2:p.Tyr185=
|
|
ENST00000345392.2:c.430T=
|
ENSP00000344757.2:p.Tyr144=
|
|
ENST00000477538.1:n.689T=
|
|
|
NM_000551.3:c.553T= , LRG_322t1:c.553T=
|
NP_000542.1:p.Tyr185=
|
|
NM_198156.2:c.430T=
|
NP_937799.1:p.Tyr144=
|
|
NM_001354723.1:c.*107T=
|
NP_001341652.1:n.*107T=
|
|
NM_000551.4:c.553T=
MANE Select
|
NP_000542.1:p.Tyr185=
|
|
NM_001354723.2:c.*107T=
|
NP_001341652.1:n.*107T=
|
|
NM_198156.3:c.430T=
|
NP_937799.1:p.Tyr144=
|
|