ENST00000334785.12:c.874G>T
MANE Select
|
ENSP00000333938.7:p.Asp292Tyr
|
|
ENST00000330010.12:c.682G>T
|
ENSP00000327363.8:p.Asp228Tyr
|
|
ENST00000334785.11:c.874G>T
|
ENSP00000333938.7:p.Asp292Tyr
|
|
ENST00000342754.5:c.573G>T
|
|
|
ENST00000401035.7:c.682G>T
|
ENSP00000383814.3:p.Asp228Tyr
|
|
ENST00000440324.5:c.832G>T
|
ENSP00000411902.1:p.Asp278Tyr
|
|
ENST00000464998.1:n.334G>T
|
|
|
NM_001172309.1:c.682G>T
|
NP_001165780.1:p.Asp228Tyr
|
|
NM_144573.3:c.874G>T , LRG_442t1:c.874G>T
|
NP_653174.3:p.Asp292Tyr
|
|
XM_005271322.2:c.874G>T
|
XP_005271379.1:p.Asp292Tyr
|
|
XM_005271323.2:c.832G>T
|
XP_005271380.1:p.Asp278Tyr
|
|
XM_005271324.3:c.682G>T
|
XP_005271381.1:p.Asp228Tyr
|
|
XM_005271325.2:c.874G>T
|
XP_005271382.1:p.Asp292Tyr
|
|
XM_005271326.2:c.640G>T
|
XP_005271383.1:p.Asp214Tyr
|
|
XM_005271327.2:c.457G>T
|
XP_005271384.1:p.Asp153Tyr
|
|
XM_005271322.4:c.874G>T
|
XP_005271379.1:p.Asp292Tyr
|
|
XM_005271323.4:c.832G>T
|
XP_005271380.1:p.Asp278Tyr
|
|
XM_005271324.5:c.682G>T
|
XP_005271381.1:p.Asp228Tyr
|
|
XM_005271325.4:c.874G>T
|
XP_005271382.1:p.Asp292Tyr
|
|
XM_005271326.4:c.640G>T
|
XP_005271383.1:p.Asp214Tyr
|
|
XM_005271327.4:c.457G>T
|
XP_005271384.1:p.Asp153Tyr
|
|
NM_001172309.2:c.682G>T
|
NP_001165780.1:p.Asp228Tyr
|
|
NM_144573.4:c.874G>T
MANE Select
|
NP_653174.3:p.Asp292Tyr
|
|