|
ENST00000380950.7:c.2978T>C
MANE Select
|
ENSP00000370337.2:p.Val993Ala
|
|
|
ENST00000325747.9:c.2699T>C
|
ENSP00000321000.5:p.Val900Ala
|
|
|
ENST00000380950.6:c.2978T>C
|
ENSP00000370337.2:p.Val993Ala
|
|
|
ENST00000399334.7:c.2978T>C
|
ENSP00000382271.3:p.Val993Ala
|
|
|
NM_001194998.1:c.2978T>C
|
NP_001181927.1:p.Val993Ala
|
|
|
NM_014985.3:c.2978T>C
|
NP_055800.2:p.Val993Ala
|
|
|
XM_006720437.2:c.2978T>C
|
XP_006720500.1:p.Val993Ala
|
|
|
XM_011521373.1:c.2978T>C
|
XP_011519675.1:p.Val993Ala
|
|
|
XM_011521374.1:c.2978T>C
|
XP_011519676.1:p.Val993Ala
|
|
|
XM_011521375.1:c.2978T>C
|
XP_011519677.1:p.Val993Ala
|
|
|
XM_011521376.1:c.2978T>C
|
XP_011519678.1:p.Val993Ala
|
|
|
XM_011521377.1:c.2978T>C
|
XP_011519679.1:p.Val993Ala
|
|
|
XM_011521378.1:c.2978T>C
|
XP_011519680.1:p.Val993Ala
|
|
|
XM_011521379.1:c.2978T>C
|
XP_011519681.1:p.Val993Ala
|
|
|
XM_011521380.1:c.1019T>C
|
XP_011519682.1:p.Val340Ala
|
|
|
XM_011521381.1:c.1013T>C
|
XP_011519683.1:p.Val338Ala
|
|
|
XR_931769.1:n.3943T>C
|
|
|
|
XR_931770.1:n.3943T>C
|
|
|
|
XR_931771.1:n.3943T>C
|
|
|
|
XR_931772.1:n.3943T>C
|
|
|
|
XR_931773.1:n.3943T>C
|
|
|
|
XR_931774.1:n.3943T>C
|
|
|
|
XR_931775.1:n.3943T>C
|
|
|
|
XM_006720437.3:c.2978T>C
|
XP_006720500.1:p.Val993Ala
|
|
|
XM_011521373.3:c.2978T>C
|
XP_011519675.1:p.Val993Ala
|
|
|
XM_011521374.3:c.2978T>C
|
XP_011519676.1:p.Val993Ala
|
|
|
XM_011521375.3:c.2978T>C
|
XP_011519677.1:p.Val993Ala
|
|
|
XM_011521378.3:c.2978T>C
|
XP_011519680.1:p.Val993Ala
|
|
|
XM_011521379.3:c.2978T>C
|
XP_011519681.1:p.Val993Ala
|
|
|
XM_011521381.2:c.1013T>C
|
XP_011519683.1:p.Val338Ala
|
|
|
XM_017022015.1:c.1013T>C
|
XP_016877504.1:p.Val338Ala
|
|
|
XM_024449875.1:c.2978T>C
|
XP_024305643.1:p.Val993Ala
|
|
|
XR_001751153.2:n.3929T>C
|
|
|
|
XR_931769.3:n.3929T>C
|
|
|
|
XR_931770.3:n.3929T>C
|
|
|
|
XR_931775.3:n.3929T>C
|
|
|
|
NM_001194998.2:c.2978T>C
MANE Select
|
NP_001181927.1:p.Val993Ala
|
|
|
NM_014985.4:c.2978T>C
|
NP_055800.2:p.Val993Ala
|
|
