ENST00000350026.11:c.4752T>G
|
ENSP00000055163.8:p.Ser1584=
|
|
ENST00000414678.8:c.4821T>G
|
ENSP00000412835.3:p.Ser1607=
|
|
ENST00000637015.2:c.5040T>G
|
ENSP00000489729.2:p.Ser1680=
|
|
ENST00000346085.10:c.4791T>G
|
ENSP00000344546.5:p.Ser1597=
|
|
ENST00000350026.10:c.4503T>G
|
ENSP00000055163.7:p.Ser1501=
|
|
ENST00000414678.7:c.3069T>G
|
ENSP00000412835.2:p.Ser1023=
|
|
ENST00000635849.1:c.2232T>G
|
ENSP00000490948.1:p.Ser744=
|
|
ENST00000635957.1:c.1863T>G
|
ENSP00000490385.1:p.Ser621=
|
|
ENST00000636227.1:n.3374T>G
|
|
|
ENST00000636254.1:n.831T>G
|
|
|
ENST00000636930.2:c.4911T>G
MANE Select
|
ENSP00000490491.2:p.Ser1637=
|
|
ENST00000636940.1:n.2908T>G
|
|
|
ENST00000637015.1:c.2279T>G
|
|
|
ENST00000637568.1:c.2193T>G
|
|
|
ENST00000637741.1:n.1577T>G
|
|
|
ENST00000637810.1:c.2253T>G
|
ENSP00000489636.1:p.Ser751=
|
|
ENST00000637904.1:c.2412T>G
|
ENSP00000490550.1:p.Ser804=
|
|
ENST00000647938.1:c.4542T>G
|
ENSP00000498155.1:p.Ser1514=
|
|
ENST00000346085.9:c.4542T>G
|
ENSP00000344546.4:p.Ser1514=
|
|
ENST00000350026.9:c.4503T>G
|
ENSP00000055163.7:p.Ser1501=
|
|
ENST00000414678.6:c.3069T>G
|
ENSP00000412835.2:p.Ser1023=
|
|
NM_017519.2:c.4503T>G
|
NP_059989.2:p.Ser1501=
|
|
NM_020732.3:c.4542T>G
|
NP_065783.3:p.Ser1514=
|
|
XM_005267069.3:c.4662T>G
|
XP_005267126.2:p.Ser1554=
|
|
XM_011535984.1:c.3741T>G
|
XP_011534286.1:p.Ser1247=
|
|
XM_011535985.1:c.3561T>G
|
XP_011534287.1:p.Ser1187=
|
|
XM_011535986.1:c.3321T>G
|
XP_011534288.1:p.Ser1107=
|
|
XM_011535987.1:c.2940T>G
|
XP_011534289.1:p.Ser980=
|
|
XM_011535988.1:c.1803T>G
|
XP_011534290.1:p.Ser601=
|
|
NM_001346813.1:c.4662T>G
|
NP_001333742.1:p.Ser1554=
|
|
NM_001363725.1:c.2412T>G
|
NP_001350654.1:p.Ser804=
|
|
XM_011535984.2:c.4872T>G
|
XP_011534286.2:p.Ser1624=
|
|
XM_011535988.3:c.1803T>G
|
XP_011534290.1:p.Ser601=
|
|
XM_017011103.2:c.4773T>G
|
XP_016866592.1:p.Ser1591=
|
|
XM_017011104.1:c.4743T>G
|
XP_016866593.1:p.Ser1581=
|
|
XM_017011105.2:c.4713T>G
|
XP_016866594.1:p.Ser1571=
|
|
XM_017011106.2:c.4584T>G
|
XP_016866595.1:p.Ser1528=
|
|
XM_017011107.2:c.4563T>G
|
XP_016866596.1:p.Ser1521=
|
|
XR_002956289.1:n.4858T>G
|
|
|
NM_001363725.2:c.2412T>G
|
NP_001350654.1:p.Ser804=
|
|
NM_001371656.1:c.4791T>G
|
NP_001358585.1:p.Ser1597=
|
|
NM_001374820.1:c.4791T>G
|
NP_001361749.1:p.Ser1597=
|
|
NM_001374828.1:c.4911T>G
MANE Select
|
NP_001361757.1:p.Ser1637=
|
|
NM_017519.3:c.4752T>G
|
NP_059989.3:p.Ser1584=
|
|