|
ENST00000689298.1:c.*3120G>T
|
ENSP00000508434.1:n.*3120G>T
|
|
|
ENST00000440875.6:c.2494G>T
|
ENSP00000475553.3:p.Ala832Ser
|
|
|
ENST00000627532.3:c.3271G>T
MANE Select
|
ENSP00000487174.1:p.Ala1091Ser
|
|
|
ENST00000636026.2:c.3230+41G>T
|
ENSP00000490776.1:n.3230+41G>T
|
|
|
ENST00000636179.1:n.3240G>T
|
|
|
|
ENST00000636413.1:c.2935G>T
|
ENSP00000490508.1:p.Ala979Ser
|
|
|
ENST00000636471.1:c.3346G>T
|
ENSP00000490317.1:p.Ala1116Ser
|
|
|
ENST00000636732.2:c.*2988G>T
|
ENSP00000490175.1:n.*2988G>T
|
|
|
ENST00000636820.1:n.3371G>T
|
|
|
|
ENST00000637045.1:c.2935G>T
|
ENSP00000490141.1:p.Ala979Ser
|
|
|
ENST00000637304.1:c.2935G>T
|
ENSP00000490872.1:p.Ala979Ser
|
|
|
ENST00000638007.1:c.2935G>T
|
ENSP00000490723.1:p.Ala979Ser
|
|
|
ENST00000638087.1:c.2935G>T
|
ENSP00000490673.1:p.Ala979Ser
|
|
|
ENST00000638128.1:c.2494G>T
|
ENSP00000490934.1:p.Ala832Ser
|
|
|
ENST00000639389.1:c.151+6587G>T
|
ENSP00000492572.1:n.151+6587G>T
|
|
|
ENST00000647488.1:c.491G>T
|
ENSP00000494820.1:n.491G>T
|
|
|
ENST00000675069.1:c.802G>T
|
ENSP00000502467.1:p.Ala268Ser
|
|
|
ENST00000303660.8:c.3268G>T
|
ENSP00000302501.4:p.Ala1090Ser
|
|
|
ENST00000409487.7:c.3271G>T
|
ENSP00000386854.2:p.Ala1091Ser
|
|
|
ENST00000419938.5:c.656-943G>T
|
ENSP00000394777.2:n.656-943G>T
|
|
|
ENST00000539609.7:c.3199G>T
|
ENSP00000443792.2:p.Ala1067Ser
|
|
|
ENST00000558170.6:c.3271G>T
|
ENSP00000454157.1:p.Ala1091Ser
|
|
|
ENST00000627532.2:c.3271G>T
|
ENSP00000487174.1:p.Ala1091Ser
|
|
|
NM_001171653.1:c.3199G>T
|
NP_001165124.1:p.Ala1067Ser
|
|
|
NM_014795.3:c.3271G>T
|
NP_055610.1:p.Ala1091Ser
|
|
|
XM_006712881.2:c.3271G>T
|
XP_006712944.1:p.Ala1091Ser
|
|
|
XM_006712882.2:c.3271G>T
|
XP_006712945.1:p.Ala1091Ser
|
|
|
XM_011512231.1:c.3262G>T
|
XP_011510533.1:p.Ala1088Ser
|
|
|
XM_011512232.1:c.3250G>T
|
XP_011510534.1:p.Ala1084Ser
|
|
|
NM_014795.4:c.3271G>T
MANE Select
|
NP_055610.1:p.Ala1091Ser
|
|
|
NM_001171653.2:c.3199G>T
|
NP_001165124.1:p.Ala1067Ser
|
|
