|
ENST00000689298.1:c.*2638G>C
|
ENSP00000508434.1:n.*2638G>C
|
|
|
ENST00000440875.6:c.2012G>C
|
ENSP00000475553.3:p.Ser671Thr
|
|
|
ENST00000627532.3:c.2789G>C
MANE Select
|
ENSP00000487174.1:p.Ser930Thr
|
|
|
ENST00000636026.2:c.2789G>C
|
ENSP00000490776.1:p.Ser930Thr
|
|
|
ENST00000636179.1:n.2758G>C
|
|
|
|
ENST00000636413.1:c.2453G>C
|
ENSP00000490508.1:p.Ser818Thr
|
|
|
ENST00000636471.1:c.2864G>C
|
ENSP00000490317.1:p.Ser955Thr
|
|
|
ENST00000636732.2:c.*2506G>C
|
ENSP00000490175.1:n.*2506G>C
|
|
|
ENST00000636820.1:n.2889G>C
|
|
|
|
ENST00000637045.1:c.2453G>C
|
ENSP00000490141.1:p.Ser818Thr
|
|
|
ENST00000637304.1:c.2453G>C
|
ENSP00000490872.1:p.Ser818Thr
|
|
|
ENST00000638007.1:c.2453G>C
|
ENSP00000490723.1:p.Ser818Thr
|
|
|
ENST00000638087.1:c.2453G>C
|
ENSP00000490673.1:p.Ser818Thr
|
|
|
ENST00000638128.1:c.2012G>C
|
ENSP00000490934.1:p.Ser671Thr
|
|
|
ENST00000675069.1:c.320G>C
|
ENSP00000502467.1:p.Ser107Thr
|
|
|
ENST00000303660.8:c.2786G>C
|
ENSP00000302501.4:p.Ser929Thr
|
|
|
ENST00000409487.7:c.2789G>C
|
ENSP00000386854.2:p.Ser930Thr
|
|
|
ENST00000419938.5:c.655+2801G>C
|
ENSP00000394777.2:n.655+2801G>C
|
|
|
ENST00000440875.5:c.1168-470G>C
|
ENSP00000475553.2:n.1168-470G>C
|
|
|
ENST00000539609.7:c.2717G>C
|
ENSP00000443792.2:p.Ser906Thr
|
|
|
ENST00000558170.6:c.2789G>C
|
ENSP00000454157.1:p.Ser930Thr
|
|
|
ENST00000627532.2:c.2789G>C
|
ENSP00000487174.1:p.Ser930Thr
|
|
|
NM_001171653.1:c.2717G>C
|
NP_001165124.1:p.Ser906Thr
|
|
|
NM_014795.3:c.2789G>C
|
NP_055610.1:p.Ser930Thr
|
|
|
XM_006712881.2:c.2789G>C
|
XP_006712944.1:p.Ser930Thr
|
|
|
XM_006712882.2:c.2789G>C
|
XP_006712945.1:p.Ser930Thr
|
|
|
XM_011512231.1:c.2780G>C
|
XP_011510533.1:p.Ser927Thr
|
|
|
XM_011512232.1:c.2768G>C
|
XP_011510534.1:p.Ser923Thr
|
|
|
NM_014795.4:c.2789G>C
MANE Select
|
NP_055610.1:p.Ser930Thr
|
|
|
NM_001171653.2:c.2717G>C
|
NP_001165124.1:p.Ser906Thr
|
|
