ENST00000261195.3:c.976C>G
MANE Select
|
ENSP00000261195.2:p.Leu326Val
|
|
ENST00000647960.1:c.*978C>G
|
ENSP00000497202.1:n.*978C>G
|
|
ENST00000648372.1:n.903C>G
|
|
|
ENST00000261195.2:c.976C>G
|
ENSP00000261195.2:p.Leu326Val
|
|
NM_021957.3:c.976C>G
|
NP_068776.2:p.Leu326Val
|
|
XM_005253352.1:c.976C>G
|
XP_005253409.1:p.Leu326Val
|
|
XM_005253354.2:c.757C>G
|
XP_005253411.1:p.Leu253Val
|
|
XM_006719062.2:c.976C>G
|
XP_006719125.1:p.Leu326Val
|
|
XM_006719063.2:c.745C>G
|
XP_006719126.1:p.Leu249Val
|
|
NM_021957.4:c.976C>G
MANE Select
|
NP_068776.2:p.Leu326Val
|
|
XM_006719063.3:c.745C>G
|
XP_006719126.1:p.Leu249Val
|
|
XM_017019245.2:c.976C>G
|
XP_016874734.1:p.Leu326Val
|
|
XM_024448960.1:c.976C>G
|
XP_024304728.1:p.Leu326Val
|
|