ENST00000399391.7:c.6383T>C
|
ENSP00000382323.2:p.Val2128Ala
|
|
ENST00000399397.6:c.6347T>C
MANE Select
|
ENSP00000382329.2:p.Val2116Ala
|
|
ENST00000342528.2:c.3401T>C
|
ENSP00000341666.2:p.Val1134Ala
|
|
ENST00000399391.6:c.6383T>C
|
ENSP00000382323.2:p.Val2128Ala
|
|
ENST00000399397.5:c.6347T>C
|
ENSP00000382329.2:p.Val2116Ala
|
|
NM_001277269.1:c.6383T>C
|
NP_001264198.1:p.Val2128Ala
|
|
NM_001292063.1:c.6347T>C
|
NP_001278992.1:p.Val2116Ala
|
|
NM_001277269.2:c.6383T>C
|
NP_001264198.1:p.Val2128Ala
|
|
NM_001292063.2:c.6347T>C
MANE Select
|
NP_001278992.1:p.Val2116Ala
|
|