ENST00000350026.11:c.3070G>T
|
ENSP00000055163.8:p.Ala1024Ser
|
|
ENST00000414678.8:c.2980G>T
|
ENSP00000412835.3:p.Ala994Ser
|
|
ENST00000637015.2:c.3070G>T
|
ENSP00000489729.2:p.Ala1024Ser
|
|
ENST00000319584.11:c.1084G>T
|
ENSP00000313006.7:p.Ala362Ser
|
|
ENST00000346085.10:c.3109G>T
|
ENSP00000344546.5:p.Ala1037Ser
|
|
ENST00000350026.10:c.2821G>T
|
ENSP00000055163.7:p.Ala941Ser
|
|
ENST00000414678.7:c.1228G>T
|
ENSP00000412835.2:p.Ala410Ser
|
|
ENST00000452544.2:n.971G>T
|
|
|
ENST00000635849.1:c.391G>T
|
ENSP00000490948.1:p.Ala131Ser
|
|
ENST00000635957.1:c.25G>T
|
ENSP00000490385.1:p.Ala9Ser
|
|
ENST00000636426.1:n.204G>T
|
|
|
ENST00000636930.2:c.3070G>T
MANE Select
|
ENSP00000490491.2:p.Ala1024Ser
|
|
ENST00000637015.1:c.309G>T
|
|
|
ENST00000637568.1:c.113G>T
|
|
|
ENST00000637810.1:c.571G>T
|
ENSP00000489636.1:p.Ala191Ser
|
|
ENST00000637904.1:c.571G>T
|
ENSP00000490550.1:p.Ala191Ser
|
|
ENST00000647938.1:c.2860G>T
|
ENSP00000498155.1:p.Ala954Ser
|
|
ENST00000674190.1:n.1819G>T
|
|
|
ENST00000319584.10:c.1087G>T
|
ENSP00000313006.6:p.Ala363Ser
|
|
ENST00000346085.9:c.2860G>T
|
ENSP00000344546.4:p.Ala954Ser
|
|
ENST00000350026.9:c.2821G>T
|
ENSP00000055163.7:p.Ala941Ser
|
|
ENST00000400790.3:c.22G>T
|
ENSP00000383596.3:p.Ala8Ser
|
|
ENST00000414678.6:c.1228G>T
|
ENSP00000412835.2:p.Ala410Ser
|
|
ENST00000452544.1:n.917G>T
|
|
|
ENST00000478761.3:c.143G>T
|
|
|
NM_017519.2:c.2821G>T
|
NP_059989.2:p.Ala941Ser
|
|
NM_020732.3:c.2860G>T
|
NP_065783.3:p.Ala954Ser
|
|
XM_005267069.3:c.2821G>T
|
XP_005267126.2:p.Ala941Ser
|
|
XM_011535984.1:c.1771G>T
|
XP_011534286.1:p.Ala591Ser
|
|
XM_011535985.1:c.1591G>T
|
XP_011534287.1:p.Ala531Ser
|
|
XM_011535986.1:c.1351G>T
|
XP_011534288.1:p.Ala451Ser
|
|
XM_011535987.1:c.970G>T
|
XP_011534289.1:p.Ala324Ser
|
|
XM_011535988.1:c.-20+15725G>T
|
XP_011534290.1:n.-20+15725G>T
|
|
NM_001346813.1:c.2821G>T
|
NP_001333742.1:p.Ala941Ser
|
|
NM_001363725.1:c.571G>T
|
NP_001350654.1:p.Ala191Ser
|
|
XM_011535984.2:c.2902G>T
|
XP_011534286.2:p.Ala968Ser
|
|
XM_011535988.3:c.-20+15725G>T
|
XP_011534290.1:n.-20+15725G>T
|
|
XM_017011103.2:c.2902G>T
|
XP_016866592.1:p.Ala968Ser
|
|
XM_017011104.1:c.2902G>T
|
XP_016866593.1:p.Ala968Ser
|
|
XM_017011105.2:c.2902G>T
|
XP_016866594.1:p.Ala968Ser
|
|
XM_017011106.2:c.2902G>T
|
XP_016866595.1:p.Ala968Ser
|
|
XM_017011107.2:c.2722G>T
|
XP_016866596.1:p.Ala908Ser
|
|
XR_002956289.1:n.2985G>T
|
|
|
NM_001363725.2:c.571G>T
|
NP_001350654.1:p.Ala191Ser
|
|
NM_001371656.1:c.3109G>T
|
NP_001358585.1:p.Ala1037Ser
|
|
NM_001374820.1:c.3109G>T
|
NP_001361749.1:p.Ala1037Ser
|
|
NM_001374828.1:c.3070G>T
MANE Select
|
NP_001361757.1:p.Ala1024Ser
|
|
NM_017519.3:c.3070G>T
|
NP_059989.3:p.Ala1024Ser
|
|