ENST00000350026.11:c.3951C>A
|
ENSP00000055163.8:p.Ser1317=
|
|
ENST00000414678.8:c.4020C>A
|
ENSP00000412835.3:p.Ser1340=
|
|
ENST00000637015.2:c.4239C>A
|
ENSP00000489729.2:p.Ser1413=
|
|
ENST00000346085.10:c.3990C>A
|
ENSP00000344546.5:p.Ser1330=
|
|
ENST00000350026.10:c.3702C>A
|
ENSP00000055163.7:p.Ser1234=
|
|
ENST00000414678.7:c.2268C>A
|
ENSP00000412835.2:p.Ser756=
|
|
ENST00000635849.1:c.1431C>A
|
ENSP00000490948.1:p.Ser477=
|
|
ENST00000635957.1:c.1062C>A
|
ENSP00000490385.1:p.Ser354=
|
|
ENST00000636930.2:c.4110C>A
MANE Select
|
ENSP00000490491.2:p.Ser1370=
|
|
ENST00000636940.1:n.2107C>A
|
|
|
ENST00000637015.1:c.1478C>A
|
|
|
ENST00000637568.1:c.1392C>A
|
|
|
ENST00000637741.1:n.776C>A
|
|
|
ENST00000637810.1:c.1452C>A
|
ENSP00000489636.1:p.Ser484=
|
|
ENST00000637904.1:c.1611C>A
|
ENSP00000490550.1:p.Ser537=
|
|
ENST00000647938.1:c.3741C>A
|
ENSP00000498155.1:p.Ser1247=
|
|
ENST00000346085.9:c.3741C>A
|
ENSP00000344546.4:p.Ser1247=
|
|
ENST00000350026.9:c.3702C>A
|
ENSP00000055163.7:p.Ser1234=
|
|
ENST00000414678.6:c.2268C>A
|
ENSP00000412835.2:p.Ser756=
|
|
NM_017519.2:c.3702C>A
|
NP_059989.2:p.Ser1234=
|
|
NM_020732.3:c.3741C>A
|
NP_065783.3:p.Ser1247=
|
|
XM_005267069.3:c.3861C>A
|
XP_005267126.2:p.Ser1287=
|
|
XM_011535984.1:c.2940C>A
|
XP_011534286.1:p.Ser980=
|
|
XM_011535985.1:c.2760C>A
|
XP_011534287.1:p.Ser920=
|
|
XM_011535986.1:c.2520C>A
|
XP_011534288.1:p.Ser840=
|
|
XM_011535987.1:c.2139C>A
|
XP_011534289.1:p.Ser713=
|
|
XM_011535988.1:c.1002C>A
|
XP_011534290.1:p.Ser334=
|
|
NM_001346813.1:c.3861C>A
|
NP_001333742.1:p.Ser1287=
|
|
NM_001363725.1:c.1611C>A
|
NP_001350654.1:p.Ser537=
|
|
XM_011535984.2:c.4071C>A
|
XP_011534286.2:p.Ser1357=
|
|
XM_011535988.3:c.1002C>A
|
XP_011534290.1:p.Ser334=
|
|
XM_017011103.2:c.3972C>A
|
XP_016866592.1:p.Ser1324=
|
|
XM_017011104.1:c.3942C>A
|
XP_016866593.1:p.Ser1314=
|
|
XM_017011105.2:c.3912C>A
|
XP_016866594.1:p.Ser1304=
|
|
XM_017011106.2:c.3783C>A
|
XP_016866595.1:p.Ser1261=
|
|
XM_017011107.2:c.3762C>A
|
XP_016866596.1:p.Ser1254=
|
|
XR_002956289.1:n.4154C>A
|
|
|
NM_001363725.2:c.1611C>A
|
NP_001350654.1:p.Ser537=
|
|
NM_001371656.1:c.3990C>A
|
NP_001358585.1:p.Ser1330=
|
|
NM_001374820.1:c.3990C>A
|
NP_001361749.1:p.Ser1330=
|
|
NM_001374828.1:c.4110C>A
MANE Select
|
NP_001361757.1:p.Ser1370=
|
|
NM_017519.3:c.3951C>A
|
NP_059989.3:p.Ser1317=
|
|