ENST00000638375.2:c.940G>T
|
ENSP00000492789.2:p.Ala314Ser
|
|
ENST00000706892.1:n.2597G>T
|
|
|
ENST00000706893.1:c.*41G>T
|
ENSP00000516609.1:n.*41G>T
|
|
ENST00000706894.1:c.1057G>T
|
ENSP00000516610.1:p.Ala353Ser
|
|
ENST00000706895.1:n.1877G>T
|
|
|
ENST00000706896.1:n.2353G>T
|
|
|
ENST00000706897.1:n.1775G>T
|
|
|
ENST00000706898.1:c.1075G>T
|
ENSP00000516611.1:p.Ala359Ser
|
|
ENST00000706899.1:n.1911G>T
|
|
|
ENST00000706900.1:c.973G>T
|
ENSP00000516617.1:p.Ala325Ser
|
|
ENST00000706901.1:c.1057G>T
|
ENSP00000516612.1:p.Ala353Ser
|
|
ENST00000706902.1:c.1057G>T
|
ENSP00000516613.1:p.Ala353Ser
|
|
ENST00000706903.1:c.1057G>T
|
ENSP00000516614.1:p.Ala353Ser
|
|
ENST00000706904.1:c.1057G>T
|
ENSP00000516615.1:p.Ala353Ser
|
|
ENST00000706905.1:c.1057G>T
|
ENSP00000516616.1:p.Ala353Ser
|
|
ENST00000376809.10:c.1057G>T
MANE Select
|
ENSP00000366005.5:p.Ala353Ser
|
|
ENST00000638375.1:c.940G>T
|
ENSP00000492789.1:p.Ala314Ser
|
|
ENST00000376802.2:c.896-206G>T
|
ENSP00000365998.2:n.896-206G>T
|
|
ENST00000376806.9:c.1075G>T
|
ENSP00000366002.5:p.Ala359Ser
|
|
ENST00000376809.9:c.1057G>T
|
ENSP00000366005.5:p.Ala353Ser
|
|
ENST00000396634.5:c.1057G>T
|
ENSP00000379873.1:p.Ala353Ser
|
|
ENST00000461903.1:n.1316G>T
|
|
|
ENST00000479320.5:n.1298G>T
|
|
|
ENST00000495183.5:n.1296G>T
|
|
|
ENST00000496081.5:n.1316G>T
|
|
|
NM_002116.7:c.1057G>T
|
NP_002107.3:p.Ala353Ser
|
|
NM_002116.8:c.1057G>T
MANE Select
|
NP_002107.3:p.Ala353Ser
|
|