ENST00000350026.11:c.4693C>A
|
ENSP00000055163.8:p.Arg1565Ser
|
|
ENST00000414678.8:c.4762C>A
|
ENSP00000412835.3:p.Arg1588Ser
|
|
ENST00000637015.2:c.4981C>A
|
ENSP00000489729.2:p.Arg1661Ser
|
|
ENST00000346085.10:c.4732C>A
|
ENSP00000344546.5:p.Arg1578Ser
|
|
ENST00000350026.10:c.4444C>A
|
ENSP00000055163.7:p.Arg1482Ser
|
|
ENST00000414678.7:c.3010C>A
|
ENSP00000412835.2:p.Arg1004Ser
|
|
ENST00000635849.1:c.2173C>A
|
ENSP00000490948.1:p.Arg725Ser
|
|
ENST00000635957.1:c.1804C>A
|
ENSP00000490385.1:p.Arg602Ser
|
|
ENST00000636227.1:n.3315C>A
|
|
|
ENST00000636254.1:n.772C>A
|
|
|
ENST00000636930.2:c.4852C>A
MANE Select
|
ENSP00000490491.2:p.Arg1618Ser
|
|
ENST00000636940.1:n.2849C>A
|
|
|
ENST00000637015.1:c.2220C>A
|
|
|
ENST00000637568.1:c.2134C>A
|
|
|
ENST00000637741.1:n.1518C>A
|
|
|
ENST00000637810.1:c.2194C>A
|
ENSP00000489636.1:p.Arg732Ser
|
|
ENST00000637904.1:c.2353C>A
|
ENSP00000490550.1:p.Arg785Ser
|
|
ENST00000647938.1:c.4483C>A
|
ENSP00000498155.1:p.Arg1495Ser
|
|
ENST00000346085.9:c.4483C>A
|
ENSP00000344546.4:p.Arg1495Ser
|
|
ENST00000350026.9:c.4444C>A
|
ENSP00000055163.7:p.Arg1482Ser
|
|
ENST00000414678.6:c.3010C>A
|
ENSP00000412835.2:p.Arg1004Ser
|
|
NM_017519.2:c.4444C>A
|
NP_059989.2:p.Arg1482Ser
|
|
NM_020732.3:c.4483C>A
|
NP_065783.3:p.Arg1495Ser
|
|
XM_005267069.3:c.4603C>A
|
XP_005267126.2:p.Arg1535Ser
|
|
XM_011535984.1:c.3682C>A
|
XP_011534286.1:p.Arg1228Ser
|
|
XM_011535985.1:c.3502C>A
|
XP_011534287.1:p.Arg1168Ser
|
|
XM_011535986.1:c.3262C>A
|
XP_011534288.1:p.Arg1088Ser
|
|
XM_011535987.1:c.2881C>A
|
XP_011534289.1:p.Arg961Ser
|
|
XM_011535988.1:c.1744C>A
|
XP_011534290.1:p.Arg582Ser
|
|
NM_001346813.1:c.4603C>A
|
NP_001333742.1:p.Arg1535Ser
|
|
NM_001363725.1:c.2353C>A
|
NP_001350654.1:p.Arg785Ser
|
|
XM_011535984.2:c.4813C>A
|
XP_011534286.2:p.Arg1605Ser
|
|
XM_011535988.3:c.1744C>A
|
XP_011534290.1:p.Arg582Ser
|
|
XM_017011103.2:c.4714C>A
|
XP_016866592.1:p.Arg1572Ser
|
|
XM_017011104.1:c.4684C>A
|
XP_016866593.1:p.Arg1562Ser
|
|
XM_017011105.2:c.4654C>A
|
XP_016866594.1:p.Arg1552Ser
|
|
XM_017011106.2:c.4525C>A
|
XP_016866595.1:p.Arg1509Ser
|
|
XM_017011107.2:c.4504C>A
|
XP_016866596.1:p.Arg1502Ser
|
|
XR_002956289.1:n.4799C>A
|
|
|
NM_001363725.2:c.2353C>A
|
NP_001350654.1:p.Arg785Ser
|
|
NM_001371656.1:c.4732C>A
|
NP_001358585.1:p.Arg1578Ser
|
|
NM_001374820.1:c.4732C>A
|
NP_001361749.1:p.Arg1578Ser
|
|
NM_001374828.1:c.4852C>A
MANE Select
|
NP_001361757.1:p.Arg1618Ser
|
|
NM_017519.3:c.4693C>A
|
NP_059989.3:p.Arg1565Ser
|
|