ENST00000700061.1:c.4401T>A
|
|
|
ENST00000700062.1:c.4426+13632T>A
|
|
|
ENST00000700063.1:c.926T>A
|
|
|
ENST00000700064.1:c.2271T>A
|
|
|
ENST00000281513.10:c.6415T>A
MANE Select
|
ENSP00000281513.5:p.Ser2139Thr
|
|
ENST00000281513.9:c.6415T>A
|
ENSP00000281513.5:p.Ser2139Thr
|
|
ENST00000417461.5:c.512+13632T>A
|
ENSP00000392421.1:n.512+13632T>A
|
|
ENST00000442506.5:c.3558T>A
|
|
|
NM_015909.3:c.6415T>A
|
NP_056993.2:p.Ser2139Thr
|
|
NR_052013.2:n.6280+13632T>A
|
|
|
XM_011510357.1:c.6286T>A
|
XP_011508659.1:p.Ser2096Thr
|
|
XM_011510358.1:c.6415T>A
|
XP_011508660.1:p.Ser2139Thr
|
|
XM_011510359.1:c.5776T>A
|
XP_011508661.1:p.Ser1926Thr
|
|
XM_011510360.1:c.4216T>A
|
XP_011508662.1:p.Ser1406Thr
|
|
XM_011510361.1:c.4207T>A
|
XP_011508663.1:p.Ser1403Thr
|
|
XM_011510357.2:c.6286T>A
|
XP_011508659.1:p.Ser2096Thr
|
|
XM_011510358.2:c.6415T>A
|
XP_011508660.1:p.Ser2139Thr
|
|
XM_011510360.2:c.4216T>A
|
XP_011508662.1:p.Ser1406Thr
|
|
XM_011510361.2:c.4207T>A
|
XP_011508663.1:p.Ser1403Thr
|
|
XM_017004317.1:c.6415T>A
|
XP_016859806.1:p.Ser2139Thr
|
|
XM_024452961.1:c.5776T>A
|
XP_024308729.1:p.Ser1926Thr
|
|
NM_015909.4:c.6415T>A
MANE Select
|
NP_056993.2:p.Ser2139Thr
|
|
NR_052013.3:n.6266+13632T>A
|
|
|