ENST00000350026.11:c.3816C>T
|
ENSP00000055163.8:p.Ser1272=
|
|
ENST00000414678.8:c.3885C>T
|
ENSP00000412835.3:p.Ser1295=
|
|
ENST00000637015.2:c.4104C>T
|
ENSP00000489729.2:p.Ser1368=
|
|
ENST00000346085.10:c.3855C>T
|
ENSP00000344546.5:p.Ser1285=
|
|
ENST00000350026.10:c.3567C>T
|
ENSP00000055163.7:p.Ser1189=
|
|
ENST00000414678.7:c.2133C>T
|
ENSP00000412835.2:p.Ser711=
|
|
ENST00000635849.1:c.1296C>T
|
ENSP00000490948.1:p.Ser432=
|
|
ENST00000635957.1:c.930C>T
|
ENSP00000490385.1:p.Ser310=
|
|
ENST00000636930.2:c.3975C>T
MANE Select
|
ENSP00000490491.2:p.Ser1325=
|
|
ENST00000636940.1:n.1972C>T
|
|
|
ENST00000637015.1:c.1343C>T
|
|
|
ENST00000637568.1:c.1257C>T
|
|
|
ENST00000637741.1:n.641C>T
|
|
|
ENST00000637810.1:c.1317C>T
|
ENSP00000489636.1:p.Ser439=
|
|
ENST00000637904.1:c.1476C>T
|
ENSP00000490550.1:p.Ser492=
|
|
ENST00000647938.1:c.3606C>T
|
ENSP00000498155.1:p.Ser1202=
|
|
ENST00000346085.9:c.3606C>T
|
ENSP00000344546.4:p.Ser1202=
|
|
ENST00000350026.9:c.3567C>T
|
ENSP00000055163.7:p.Ser1189=
|
|
ENST00000414678.6:c.2133C>T
|
ENSP00000412835.2:p.Ser711=
|
|
NM_017519.2:c.3567C>T
|
NP_059989.2:p.Ser1189=
|
|
NM_020732.3:c.3606C>T
|
NP_065783.3:p.Ser1202=
|
|
XM_005267069.3:c.3726C>T
|
XP_005267126.2:p.Ser1242=
|
|
XM_011535984.1:c.2805C>T
|
XP_011534286.1:p.Ser935=
|
|
XM_011535985.1:c.2625C>T
|
XP_011534287.1:p.Ser875=
|
|
XM_011535986.1:c.2385C>T
|
XP_011534288.1:p.Ser795=
|
|
XM_011535987.1:c.2004C>T
|
XP_011534289.1:p.Ser668=
|
|
XM_011535988.1:c.867C>T
|
XP_011534290.1:p.Ser289=
|
|
NM_001346813.1:c.3726C>T
|
NP_001333742.1:p.Ser1242=
|
|
NM_001363725.1:c.1476C>T
|
NP_001350654.1:p.Ser492=
|
|
XM_011535984.2:c.3936C>T
|
XP_011534286.2:p.Ser1312=
|
|
XM_011535988.3:c.867C>T
|
XP_011534290.1:p.Ser289=
|
|
XM_017011103.2:c.3837C>T
|
XP_016866592.1:p.Ser1279=
|
|
XM_017011104.1:c.3807C>T
|
XP_016866593.1:p.Ser1269=
|
|
XM_017011105.2:c.3777C>T
|
XP_016866594.1:p.Ser1259=
|
|
XM_017011106.2:c.3648C>T
|
XP_016866595.1:p.Ser1216=
|
|
XM_017011107.2:c.3627C>T
|
XP_016866596.1:p.Ser1209=
|
|
XR_002956289.1:n.4019C>T
|
|
|
NM_001363725.2:c.1476C>T
|
NP_001350654.1:p.Ser492=
|
|
NM_001371656.1:c.3855C>T
|
NP_001358585.1:p.Ser1285=
|
|
NM_001374820.1:c.3855C>T
|
NP_001361749.1:p.Ser1285=
|
|
NM_001374828.1:c.3975C>T
MANE Select
|
NP_001361757.1:p.Ser1325=
|
|
NM_017519.3:c.3816C>T
|
NP_059989.3:p.Ser1272=
|
|