ENST00000559133.6:c.*1132T>C
|
ENSP00000453958.2:n.*1132T>C
|
|
ENST00000674301.2:c.*1837T>C
|
ENSP00000501333.2:n.*1837T>C
|
|
ENST00000682158.1:n.1705T>C
|
|
|
ENST00000682170.1:n.2505T>C
|
|
|
ENST00000682767.1:n.1621T>C
|
|
|
ENST00000316623.10:c.8324T>C
MANE Select
|
ENSP00000325527.5:p.Val2775Ala
|
|
ENST00000674301.1:c.3490T>C
|
ENSP00000501333.1:n.3490T>C
|
|
ENST00000316623.9:c.8324T>C
|
ENSP00000325527.5:p.Val2775Ala
|
|
ENST00000559133.5:c.3693T>C
|
|
|
ENST00000561429.1:n.579T>C
|
|
|
NM_000138.4:c.8324T>C , LRG_778t1:c.8324T>C
|
NP_000129.3:p.Val2775Ala
|
|
NM_000138.5:c.8324T>C
MANE Select
|
NP_000129.3:p.Val2775Ala
|
|