ENST00000281928.9:c.5121C>G
MANE Select
|
ENSP00000281928.3:p.Tyr1707Ter
|
|
ENST00000549786.2:c.4549C>G
|
|
|
ENST00000648379.1:n.3489C>G
|
|
|
ENST00000648737.1:n.4885C>G
|
|
|
ENST00000648825.1:n.1861C>G
|
|
|
ENST00000648916.1:n.3132C>G
|
|
|
ENST00000649146.1:n.2364C>G
|
|
|
ENST00000649607.1:c.3305C>G
|
|
|
ENST00000649775.1:c.1610C>G
|
|
|
ENST00000650226.1:c.5121C>G
|
ENSP00000496981.1:p.Tyr1707Ter
|
|
ENST00000281928.7:c.5121C>G
|
ENSP00000281928.3:p.Tyr1707Ter
|
|
ENST00000549786.1:c.485C>G
|
|
|
ENST00000552340.1:c.153C>G
|
ENSP00000449876.1:p.Tyr51Ter
|
|
NM_015335.4:c.5121C>G
|
NP_056150.1:p.Tyr1707Ter
|
|
XM_011538080.1:c.5121C>G
|
XP_011536382.1:p.Tyr1707Ter
|
|
XM_011538081.1:c.5118C>G
|
XP_011536383.1:p.Tyr1706Ter
|
|
XM_011538082.1:c.5091C>G
|
XP_011536384.1:p.Tyr1697Ter
|
|
XM_011538080.2:c.5121C>G
|
XP_011536382.1:p.Tyr1707Ter
|
|
XM_011538081.2:c.5118C>G
|
XP_011536383.1:p.Tyr1706Ter
|
|
XM_011538082.2:c.5091C>G
|
XP_011536384.1:p.Tyr1697Ter
|
|
XM_017019090.1:c.5118C>G
|
XP_016874579.1:p.Tyr1706Ter
|
|
NM_015335.5:c.5121C>G
MANE Select
|
NP_056150.1:p.Tyr1707Ter
|
|