ENST00000281928.9:c.5038T>G
MANE Select
|
ENSP00000281928.3:p.Tyr1680Asp
|
|
ENST00000549786.2:c.4466T>G
|
|
|
ENST00000648379.1:n.3406T>G
|
|
|
ENST00000648737.1:n.4802T>G
|
|
|
ENST00000648825.1:n.1778T>G
|
|
|
ENST00000648916.1:n.3049T>G
|
|
|
ENST00000649146.1:n.2281T>G
|
|
|
ENST00000649607.1:c.3222T>G
|
|
|
ENST00000649775.1:c.1527T>G
|
|
|
ENST00000650226.1:c.5038T>G
|
ENSP00000496981.1:p.Tyr1680Asp
|
|
ENST00000281928.7:c.5038T>G
|
ENSP00000281928.3:p.Tyr1680Asp
|
|
ENST00000549786.1:c.402T>G
|
|
|
ENST00000552340.1:c.70T>G
|
ENSP00000449876.1:p.Tyr24Asp
|
|
NM_015335.4:c.5038T>G
|
NP_056150.1:p.Tyr1680Asp
|
|
XM_011538080.1:c.5038T>G
|
XP_011536382.1:p.Tyr1680Asp
|
|
XM_011538081.1:c.5035T>G
|
XP_011536383.1:p.Tyr1679Asp
|
|
XM_011538082.1:c.5008T>G
|
XP_011536384.1:p.Tyr1670Asp
|
|
XM_011538080.2:c.5038T>G
|
XP_011536382.1:p.Tyr1680Asp
|
|
XM_011538081.2:c.5035T>G
|
XP_011536383.1:p.Tyr1679Asp
|
|
XM_011538082.2:c.5008T>G
|
XP_011536384.1:p.Tyr1670Asp
|
|
XM_017019090.1:c.5035T>G
|
XP_016874579.1:p.Tyr1679Asp
|
|
NM_015335.5:c.5038T>G
MANE Select
|
NP_056150.1:p.Tyr1680Asp
|
|