ENST00000350026.11:c.3814T>G
|
ENSP00000055163.8:p.Ser1272Ala
|
|
ENST00000414678.8:c.3883T>G
|
ENSP00000412835.3:p.Ser1295Ala
|
|
ENST00000637015.2:c.4102T>G
|
ENSP00000489729.2:p.Ser1368Ala
|
|
ENST00000346085.10:c.3853T>G
|
ENSP00000344546.5:p.Ser1285Ala
|
|
ENST00000350026.10:c.3565T>G
|
ENSP00000055163.7:p.Ser1189Ala
|
|
ENST00000414678.7:c.2131T>G
|
ENSP00000412835.2:p.Ser711Ala
|
|
ENST00000635849.1:c.1294T>G
|
ENSP00000490948.1:p.Ser432Ala
|
|
ENST00000635957.1:c.928T>G
|
ENSP00000490385.1:p.Ser310Ala
|
|
ENST00000636930.2:c.3973T>G
MANE Select
|
ENSP00000490491.2:p.Ser1325Ala
|
|
ENST00000636940.1:n.1970T>G
|
|
|
ENST00000637015.1:c.1341T>G
|
|
|
ENST00000637568.1:c.1255T>G
|
|
|
ENST00000637741.1:n.639T>G
|
|
|
ENST00000637810.1:c.1315T>G
|
ENSP00000489636.1:p.Ser439Ala
|
|
ENST00000637904.1:c.1474T>G
|
ENSP00000490550.1:p.Ser492Ala
|
|
ENST00000647938.1:c.3604T>G
|
ENSP00000498155.1:p.Ser1202Ala
|
|
ENST00000346085.9:c.3604T>G
|
ENSP00000344546.4:p.Ser1202Ala
|
|
ENST00000350026.9:c.3565T>G
|
ENSP00000055163.7:p.Ser1189Ala
|
|
ENST00000414678.6:c.2131T>G
|
ENSP00000412835.2:p.Ser711Ala
|
|
NM_017519.2:c.3565T>G
|
NP_059989.2:p.Ser1189Ala
|
|
NM_020732.3:c.3604T>G
|
NP_065783.3:p.Ser1202Ala
|
|
XM_005267069.3:c.3724T>G
|
XP_005267126.2:p.Ser1242Ala
|
|
XM_011535984.1:c.2803T>G
|
XP_011534286.1:p.Ser935Ala
|
|
XM_011535985.1:c.2623T>G
|
XP_011534287.1:p.Ser875Ala
|
|
XM_011535986.1:c.2383T>G
|
XP_011534288.1:p.Ser795Ala
|
|
XM_011535987.1:c.2002T>G
|
XP_011534289.1:p.Ser668Ala
|
|
XM_011535988.1:c.865T>G
|
XP_011534290.1:p.Ser289Ala
|
|
NM_001346813.1:c.3724T>G
|
NP_001333742.1:p.Ser1242Ala
|
|
NM_001363725.1:c.1474T>G
|
NP_001350654.1:p.Ser492Ala
|
|
XM_011535984.2:c.3934T>G
|
XP_011534286.2:p.Ser1312Ala
|
|
XM_011535988.3:c.865T>G
|
XP_011534290.1:p.Ser289Ala
|
|
XM_017011103.2:c.3835T>G
|
XP_016866592.1:p.Ser1279Ala
|
|
XM_017011104.1:c.3805T>G
|
XP_016866593.1:p.Ser1269Ala
|
|
XM_017011105.2:c.3775T>G
|
XP_016866594.1:p.Ser1259Ala
|
|
XM_017011106.2:c.3646T>G
|
XP_016866595.1:p.Ser1216Ala
|
|
XM_017011107.2:c.3625T>G
|
XP_016866596.1:p.Ser1209Ala
|
|
XR_002956289.1:n.4017T>G
|
|
|
NM_001363725.2:c.1474T>G
|
NP_001350654.1:p.Ser492Ala
|
|
NM_001371656.1:c.3853T>G
|
NP_001358585.1:p.Ser1285Ala
|
|
NM_001374820.1:c.3853T>G
|
NP_001361749.1:p.Ser1285Ala
|
|
NM_001374828.1:c.3973T>G
MANE Select
|
NP_001361757.1:p.Ser1325Ala
|
|
NM_017519.3:c.3814T>G
|
NP_059989.3:p.Ser1272Ala
|
|