ENST00000350026.11:c.3932C>A
|
ENSP00000055163.8:p.Ser1311Ter
|
|
ENST00000414678.8:c.4001C>A
|
ENSP00000412835.3:p.Ser1334Ter
|
|
ENST00000637015.2:c.4220C>A
|
ENSP00000489729.2:p.Ser1407Ter
|
|
ENST00000346085.10:c.3971C>A
|
ENSP00000344546.5:p.Ser1324Ter
|
|
ENST00000350026.10:c.3683C>A
|
ENSP00000055163.7:p.Ser1228Ter
|
|
ENST00000414678.7:c.2249C>A
|
ENSP00000412835.2:p.Ser750Ter
|
|
ENST00000635849.1:c.1412C>A
|
ENSP00000490948.1:p.Ser471Ter
|
|
ENST00000635957.1:c.1043C>A
|
ENSP00000490385.1:p.Ser348Ter
|
|
ENST00000636930.2:c.4091C>A
MANE Select
|
ENSP00000490491.2:p.Ser1364Ter
|
|
ENST00000636940.1:n.2088C>A
|
|
|
ENST00000637015.1:c.1459C>A
|
|
|
ENST00000637568.1:c.1373C>A
|
|
|
ENST00000637741.1:n.757C>A
|
|
|
ENST00000637810.1:c.1433C>A
|
ENSP00000489636.1:p.Ser478Ter
|
|
ENST00000637904.1:c.1592C>A
|
ENSP00000490550.1:p.Ser531Ter
|
|
ENST00000647938.1:c.3722C>A
|
ENSP00000498155.1:p.Ser1241Ter
|
|
ENST00000346085.9:c.3722C>A
|
ENSP00000344546.4:p.Ser1241Ter
|
|
ENST00000350026.9:c.3683C>A
|
ENSP00000055163.7:p.Ser1228Ter
|
|
ENST00000414678.6:c.2249C>A
|
ENSP00000412835.2:p.Ser750Ter
|
|
NM_017519.2:c.3683C>A
|
NP_059989.2:p.Ser1228Ter
|
|
NM_020732.3:c.3722C>A
|
NP_065783.3:p.Ser1241Ter
|
|
XM_005267069.3:c.3842C>A
|
XP_005267126.2:p.Ser1281Ter
|
|
XM_011535984.1:c.2921C>A
|
XP_011534286.1:p.Ser974Ter
|
|
XM_011535985.1:c.2741C>A
|
XP_011534287.1:p.Ser914Ter
|
|
XM_011535986.1:c.2501C>A
|
XP_011534288.1:p.Ser834Ter
|
|
XM_011535987.1:c.2120C>A
|
XP_011534289.1:p.Ser707Ter
|
|
XM_011535988.1:c.983C>A
|
XP_011534290.1:p.Ser328Ter
|
|
NM_001346813.1:c.3842C>A
|
NP_001333742.1:p.Ser1281Ter
|
|
NM_001363725.1:c.1592C>A
|
NP_001350654.1:p.Ser531Ter
|
|
XM_011535984.2:c.4052C>A
|
XP_011534286.2:p.Ser1351Ter
|
|
XM_011535988.3:c.983C>A
|
XP_011534290.1:p.Ser328Ter
|
|
XM_017011103.2:c.3953C>A
|
XP_016866592.1:p.Ser1318Ter
|
|
XM_017011104.1:c.3923C>A
|
XP_016866593.1:p.Ser1308Ter
|
|
XM_017011105.2:c.3893C>A
|
XP_016866594.1:p.Ser1298Ter
|
|
XM_017011106.2:c.3764C>A
|
XP_016866595.1:p.Ser1255Ter
|
|
XM_017011107.2:c.3743C>A
|
XP_016866596.1:p.Ser1248Ter
|
|
XR_002956289.1:n.4135C>A
|
|
|
NM_001363725.2:c.1592C>A
|
NP_001350654.1:p.Ser531Ter
|
|
NM_001371656.1:c.3971C>A
|
NP_001358585.1:p.Ser1324Ter
|
|
NM_001374820.1:c.3971C>A
|
NP_001361749.1:p.Ser1324Ter
|
|
NM_001374828.1:c.4091C>A
MANE Select
|
NP_001361757.1:p.Ser1364Ter
|
|
NM_017519.3:c.3932C>A
|
NP_059989.3:p.Ser1311Ter
|
|