ENST00000350026.11:c.3444C>G
|
ENSP00000055163.8:p.Thr1148=
|
|
ENST00000414678.8:c.3513C>G
|
ENSP00000412835.3:p.Thr1171=
|
|
ENST00000637015.2:c.3732C>G
|
ENSP00000489729.2:p.Thr1244=
|
|
ENST00000319584.11:c.1617C>G
|
ENSP00000313006.7:p.Thr539=
|
|
ENST00000346085.10:c.3483C>G
|
ENSP00000344546.5:p.Thr1161=
|
|
ENST00000350026.10:c.3195C>G
|
ENSP00000055163.7:p.Thr1065=
|
|
ENST00000414678.7:c.1761C>G
|
ENSP00000412835.2:p.Thr587=
|
|
ENST00000635849.1:c.924C>G
|
ENSP00000490948.1:p.Thr308=
|
|
ENST00000635957.1:c.558C>G
|
ENSP00000490385.1:p.Thr186=
|
|
ENST00000636930.2:c.3603C>G
MANE Select
|
ENSP00000490491.2:p.Thr1201=
|
|
ENST00000636940.1:n.1600C>G
|
|
|
ENST00000637015.1:c.971C>G
|
|
|
ENST00000637568.1:c.885C>G
|
|
|
ENST00000637741.1:n.269C>G
|
|
|
ENST00000637810.1:c.945C>G
|
ENSP00000489636.1:p.Thr315=
|
|
ENST00000637904.1:c.1104C>G
|
ENSP00000490550.1:p.Thr368=
|
|
ENST00000647938.1:c.3234C>G
|
ENSP00000498155.1:p.Thr1078=
|
|
ENST00000319584.10:c.1620C>G
|
ENSP00000313006.6:p.Thr540=
|
|
ENST00000346085.9:c.3234C>G
|
ENSP00000344546.4:p.Thr1078=
|
|
ENST00000350026.9:c.3195C>G
|
ENSP00000055163.7:p.Thr1065=
|
|
ENST00000400790.3:c.396C>G
|
ENSP00000383596.3:p.Thr132=
|
|
ENST00000414678.6:c.1761C>G
|
ENSP00000412835.2:p.Thr587=
|
|
ENST00000478761.3:c.805C>G
|
|
|
NM_017519.2:c.3195C>G
|
NP_059989.2:p.Thr1065=
|
|
NM_020732.3:c.3234C>G
|
NP_065783.3:p.Thr1078=
|
|
XM_005267069.3:c.3354C>G
|
XP_005267126.2:p.Thr1118=
|
|
XM_011535984.1:c.2433C>G
|
XP_011534286.1:p.Thr811=
|
|
XM_011535985.1:c.2253C>G
|
XP_011534287.1:p.Thr751=
|
|
XM_011535986.1:c.2013C>G
|
XP_011534288.1:p.Thr671=
|
|
XM_011535987.1:c.1632C>G
|
XP_011534289.1:p.Thr544=
|
|
XM_011535988.1:c.495C>G
|
XP_011534290.1:p.Thr165=
|
|
NM_001346813.1:c.3354C>G
|
NP_001333742.1:p.Thr1118=
|
|
NM_001363725.1:c.1104C>G
|
NP_001350654.1:p.Thr368=
|
|
XM_011535984.2:c.3564C>G
|
XP_011534286.2:p.Thr1188=
|
|
XM_011535988.3:c.495C>G
|
XP_011534290.1:p.Thr165=
|
|
XM_017011103.2:c.3465C>G
|
XP_016866592.1:p.Thr1155=
|
|
XM_017011104.1:c.3435C>G
|
XP_016866593.1:p.Thr1145=
|
|
XM_017011105.2:c.3405C>G
|
XP_016866594.1:p.Thr1135=
|
|
XM_017011106.2:c.3276C>G
|
XP_016866595.1:p.Thr1092=
|
|
XM_017011107.2:c.3255C>G
|
XP_016866596.1:p.Thr1085=
|
|
XR_002956289.1:n.3647C>G
|
|
|
NM_001363725.2:c.1104C>G
|
NP_001350654.1:p.Thr368=
|
|
NM_001371656.1:c.3483C>G
|
NP_001358585.1:p.Thr1161=
|
|
NM_001374820.1:c.3483C>G
|
NP_001361749.1:p.Thr1161=
|
|
NM_001374828.1:c.3603C>G
MANE Select
|
NP_001361757.1:p.Thr1201=
|
|
NM_017519.3:c.3444C>G
|
NP_059989.3:p.Thr1148=
|
|