ENST00000309755.9:c.1460T>C
MANE Select
|
ENSP00000312397.4:p.Val487Ala
|
|
ENST00000309755.8:c.1460T>C
|
ENSP00000312397.4:p.Val487Ala
|
|
ENST00000447439.6:n.1516T>C
|
|
|
ENST00000504208.5:c.*344T>C
|
ENSP00000423585.1:n.*344T>C
|
|
ENST00000506491.5:c.1214T>C
|
ENSP00000424828.1:p.Val405Ala
|
|
ENST00000506873.5:n.983T>C
|
|
|
ENST00000508657.5:c.1364T>C
|
ENSP00000422099.1:p.Val455Ala
|
|
ENST00000509694.1:n.253T>C
|
|
|
NM_001257194.1:c.1364T>C
|
NP_001244123.1:p.Val455Ala
|
|
NM_001257195.1:c.1214T>C
|
NP_001244124.1:p.Val405Ala
|
|
NM_017415.2:c.1460T>C
|
NP_059111.2:p.Val487Ala
|
|
NM_017415.3:c.1460T>C
MANE Select
|
NP_059111.2:p.Val487Ala
|
|
NM_001257195.2:c.1214T>C
|
NP_001244124.1:p.Val405Ala
|
|