|
NM_024753.5:c.3702T>G
MANE Select
|
NP_079029.3:p.Tyr1234Ter
|
|
ENST00000243344.8:c.3702T>G
MANE Select
|
ENSP00000243344.7:p.Tyr1234Ter
|
|
NM_024753.4:c.3702T>G
|
NP_079029.3:p.Tyr1234Ter
|
|
ENST00000243344.7:c.3702T>G
|
ENSP00000243344.7:p.Tyr1234Ter
|
|
ENST00000392695.6:c.602T>G
|
|
|
ENST00000497425.1:n.180T>G
|
|
|
ENST00000497425.2:n.811T>G
|
|
|
ENST00000652557.1:c.3702T>G
|
ENSP00000498617.1:p.Tyr1234Ter
|
|
ENST00000679356.1:c.3699T>G
|
ENSP00000506245.1:p.Tyr1233Ter
|
|
ENST00000679676.1:c.3591T>G
|
ENSP00000505492.1:p.Tyr1197Ter
|
|
ENST00000679799.1:c.3702T>G
|
ENSP00000505208.1:p.Tyr1234Ter
|
|
ENST00000679840.1:c.3702T>G
|
ENSP00000505248.1:p.Tyr1234Ter
|
|
ENST00000679931.1:c.*2744T>G
|
ENSP00000505632.1:n.*2744T>G
|
|
ENST00000679967.1:c.3693T>G
|
ENSP00000506607.1:p.Tyr1231Ter
|
|
ENST00000680327.1:c.*2744T>G
|
ENSP00000506639.1:n.*2744T>G
|
|
ENST00000680657.1:n.3813T>G
|
|
|
ENST00000680690.1:c.*2954T>G
|
ENSP00000506121.1:n.*2954T>G
|
|
ENST00000680888.1:c.3702T>G
|
ENSP00000506276.1:p.Tyr1234Ter
|
|
ENST00000680925.1:n.1732T>G
|
|
|
ENST00000680947.1:c.*2974T>G
|
ENSP00000506496.1:n.*2974T>G
|
|
ENST00000681024.1:c.3702T>G
|
ENSP00000506449.1:p.Tyr1234Ter
|
|
ENST00000681083.1:c.*3433T>G
|
ENSP00000506095.1:n.*3433T>G
|
|
ENST00000681167.1:n.3580T>G
|
|
|
ENST00000681483.1:c.*512T>G
|
ENSP00000505499.1:n.*512T>G
|
|
ENST00000681502.1:c.*6962T>G
|
ENSP00000505644.1:n.*6962T>G
|
|
ENST00000681819.1:c.*512T>G
|
ENSP00000505673.1:n.*512T>G
|
|
ENST00000681952.1:c.3702T>G
|
ENSP00000506400.1:p.Tyr1234Ter
|
|
XM_011511870.1:c.3135T>G
|
XP_011510172.1:p.Tyr1045Ter
|
|
XM_011511871.1:c.2952T>G
|
XP_011510173.1:p.Tyr984Ter
|
|
XM_011511871.3:c.2952T>G
|
XP_011510173.1:p.Tyr984Ter
|
|
XM_011511872.2:c.*904T>G
|
XP_011510174.1:n.*904T>G
|
|
XM_017004967.1:c.3702T>G
|
XP_016860456.1:p.Tyr1234Ter
|
|
XM_017004968.2:c.3048T>G
|
XP_016860457.1:p.Tyr1016Ter
|
|
XM_017004969.1:c.2703T>G
|
XP_016860458.1:p.Tyr901Ter
|
