ENST00000380950.7:c.314G>A
MANE Select
|
ENSP00000370337.2:p.Trp105Ter
|
|
ENST00000325747.9:c.261+134G>A
|
ENSP00000321000.5:n.261+134G>A
|
|
ENST00000380950.6:c.314G>A
|
ENSP00000370337.2:p.Trp105Ter
|
|
ENST00000399334.7:c.314G>A
|
ENSP00000382271.3:p.Trp105Ter
|
|
ENST00000560322.5:c.314G>A
|
ENSP00000453440.1:p.Trp105Ter
|
|
NM_001194998.1:c.314G>A
|
NP_001181927.1:p.Trp105Ter
|
|
NM_014985.3:c.314G>A
|
NP_055800.2:p.Trp105Ter
|
|
XM_006720437.2:c.314G>A
|
XP_006720500.1:p.Trp105Ter
|
|
XM_011521373.1:c.314G>A
|
XP_011519675.1:p.Trp105Ter
|
|
XM_011521374.1:c.314G>A
|
XP_011519676.1:p.Trp105Ter
|
|
XM_011521375.1:c.314G>A
|
XP_011519677.1:p.Trp105Ter
|
|
XM_011521376.1:c.314G>A
|
XP_011519678.1:p.Trp105Ter
|
|
XM_011521377.1:c.314G>A
|
XP_011519679.1:p.Trp105Ter
|
|
XM_011521378.1:c.314G>A
|
XP_011519680.1:p.Trp105Ter
|
|
XM_011521379.1:c.314G>A
|
XP_011519681.1:p.Trp105Ter
|
|
XR_931769.1:n.1279G>A
|
|
|
XR_931770.1:n.1279G>A
|
|
|
XR_931771.1:n.1279G>A
|
|
|
XR_931772.1:n.1279G>A
|
|
|
XR_931773.1:n.1279G>A
|
|
|
XR_931774.1:n.1279G>A
|
|
|
XR_931775.1:n.1279G>A
|
|
|
XM_006720437.3:c.314G>A
|
XP_006720500.1:p.Trp105Ter
|
|
XM_011521373.3:c.314G>A
|
XP_011519675.1:p.Trp105Ter
|
|
XM_011521374.3:c.314G>A
|
XP_011519676.1:p.Trp105Ter
|
|
XM_011521375.3:c.314G>A
|
XP_011519677.1:p.Trp105Ter
|
|
XM_011521378.3:c.314G>A
|
XP_011519680.1:p.Trp105Ter
|
|
XM_011521379.3:c.314G>A
|
XP_011519681.1:p.Trp105Ter
|
|
XM_017022016.2:c.314G>A
|
XP_016877505.1:p.Trp105Ter
|
|
XM_024449875.1:c.314G>A
|
XP_024305643.1:p.Trp105Ter
|
|
XR_001751153.2:n.1265G>A
|
|
|
XR_931769.3:n.1265G>A
|
|
|
XR_931770.3:n.1265G>A
|
|
|
XR_931775.3:n.1265G>A
|
|
|
NM_001194998.2:c.314G>A
MANE Select
|
NP_001181927.1:p.Trp105Ter
|
|
NM_014985.4:c.314G>A
|
NP_055800.2:p.Trp105Ter
|
|