ENST00000642496.1:c.3907C>G
|
|
|
ENST00000644397.2:c.5048C>G
MANE Select
|
ENSP00000495195.1:p.Thr1683Arg
|
|
ENST00000373965.6:c.4859C>G
|
ENSP00000363076.3:p.Thr1620Arg
|
|
ENST00000414778.5:c.4856C>G
|
ENSP00000410304.2:p.Thr1619Arg
|
|
ENST00000495484.5:c.1076C>G
|
ENSP00000480780.1:p.Thr359Arg
|
|
ENST00000614895.4:c.4871C>G
|
ENSP00000478512.1:p.Thr1624Arg
|
|
ENST00000616114.4:c.4853C>G
|
ENSP00000483745.1:p.Thr1618Arg
|
|
ENST00000618301.4:c.1208C>G
|
ENSP00000482780.1:p.Thr403Arg
|
|
ENST00000621708.4:c.4874C>G
|
ENSP00000484454.1:p.Thr1625Arg
|
|
NM_001142771.1:c.4874C>G
|
NP_001136243.1:p.Thr1625Arg
|
|
NM_001142772.1:c.4859C>G
|
NP_001136244.1:p.Thr1620Arg
|
|
NM_001354420.1:c.4853C>G
|
NP_001341349.1:p.Thr1618Arg
|
|
NM_001354429.1:c.4982C>G
|
NP_001341358.1:p.Thr1661Arg
|
|
XR_001747192.2:n.11340C>G
|
|
|
XR_001747193.2:n.11331C>G
|
|
|
NM_001142771.2:c.4874C>G
|
NP_001136243.1:p.Thr1625Arg
|
|
NM_001142772.2:c.4859C>G
|
NP_001136244.1:p.Thr1620Arg
|
|
NM_001354420.2:c.4853C>G
|
NP_001341349.1:p.Thr1618Arg
|
|
NM_001354429.2:c.4982C>G
|
NP_001341358.1:p.Thr1661Arg
|
|
NM_001384140.1:c.5048C>G
MANE Select
|
NP_001371069.1:p.Thr1683Arg
|
|