ENST00000374552.9:c.903C>G
MANE Select
|
ENSP00000363680.4:p.Tyr301Ter
|
|
ENST00000374552.8:c.903C>G
|
ENSP00000363680.4:p.Tyr301Ter
|
|
ENST00000374553.6:c.903C>G
|
ENSP00000363681.2:p.Tyr301Ter
|
|
ENST00000524573.5:c.894C>G
|
ENSP00000432585.1:p.Tyr298Ter
|
|
ENST00000616899.1:c.507C>G
|
ENSP00000481963.1:p.Tyr169Ter
|
|
NM_001005609.1:c.903C>G
|
NP_001005609.1:p.Tyr301Ter
|
|
NM_001005612.2:c.894C>G
|
NP_001005612.2:p.Tyr298Ter
|
|
NM_001399.4:c.903C>G
|
NP_001390.1:p.Tyr301Ter
|
|
XM_006724630.2:c.894C>G
|
XP_006724693.1:p.Tyr298Ter
|
|
XM_011530885.1:c.903C>G
|
XP_011529187.1:p.Tyr301Ter
|
|
XM_011530885.2:c.903C>G
|
XP_011529187.1:p.Tyr301Ter
|
|
XM_017029336.1:c.882+21C>G
|
XP_016884825.1:n.882+21C>G
|
|
NM_001399.5:c.903C>G
MANE Select
|
NP_001390.1:p.Tyr301Ter
|
|
NM_001005609.2:c.903C>G
|
NP_001005609.1:p.Tyr301Ter
|
|
NM_001005612.3:c.894C>G
|
NP_001005612.2:p.Tyr298Ter
|
|