ENST00000559133.6:c.5885A>T
|
ENSP00000453958.2:p.Tyr1962Phe
|
|
ENST00000674301.2:c.5885A>T
|
ENSP00000501333.2:p.Tyr1962Phe
|
|
ENST00000684448.1:n.4559A>T
|
|
|
ENST00000316623.10:c.5885A>T
MANE Select
|
ENSP00000325527.5:p.Tyr1962Phe
|
|
ENST00000674301.1:c.884A>T
|
ENSP00000501333.1:p.Tyr295Phe
|
|
ENST00000316623.9:c.5885A>T
|
ENSP00000325527.5:p.Tyr1962Phe
|
|
ENST00000537463.6:c.*1648A>T
|
ENSP00000440294.2:n.*1648A>T
|
|
ENST00000559133.5:c.1192A>T
|
|
|
ENST00000560820.1:n.5A>T
|
|
|
NM_000138.4:c.5885A>T , LRG_778t1:c.5885A>T
|
NP_000129.3:p.Tyr1962Phe
|
|
NM_000138.5:c.5885A>T
MANE Select
|
NP_000129.3:p.Tyr1962Phe
|
|