ENST00000559133.6:c.*693T>C
|
ENSP00000453958.2:n.*693T>C
|
|
ENST00000674301.2:c.*1398T>C
|
ENSP00000501333.2:n.*1398T>C
|
|
ENST00000682158.1:n.1266T>C
|
|
|
ENST00000682170.1:n.2066T>C
|
|
|
ENST00000682767.1:n.1182T>C
|
|
|
ENST00000316623.10:c.7885T>C
MANE Select
|
ENSP00000325527.5:p.Tyr2629His
|
|
ENST00000674301.1:c.3051T>C
|
ENSP00000501333.1:n.3051T>C
|
|
ENST00000316623.9:c.7885T>C
|
ENSP00000325527.5:p.Tyr2629His
|
|
ENST00000559133.5:c.3254T>C
|
|
|
ENST00000561429.1:n.140T>C
|
|
|
NM_000138.4:c.7885T>C , LRG_778t1:c.7885T>C
|
NP_000129.3:p.Tyr2629His
|
|
NM_000138.5:c.7885T>C
MANE Select
|
NP_000129.3:p.Tyr2629His
|
|