ENST00000706952.1:c.3073C>G
|
ENSP00000516672.1:p.Leu1025Val
|
|
ENST00000638521.1:c.866C>G
|
|
|
ENST00000638869.1:c.375C>G
|
|
|
ENST00000639642.1:c.204C>G
|
|
|
ENST00000640694.1:c.2914C>G
|
ENSP00000492403.1:p.Leu972Val
|
|
ENST00000642864.1:c.2914C>G
MANE Select
|
ENSP00000495726.1:p.Leu972Val
|
|
ENST00000674510.1:c.2914C>G
|
ENSP00000502054.1:p.Leu972Val
|
|
ENST00000674761.1:n.1221C>G
|
|
|
ENST00000675719.1:c.2884C>G
|
ENSP00000501927.1:p.Leu962Val
|
|
ENST00000375365.2:c.2299C>G
|
ENSP00000364514.2:p.Leu767Val
|
|
ENST00000396435.7:c.2914C>G
|
ENSP00000379712.3:p.Leu972Val
|
|
NM_001111125.2:c.2914C>G
|
NP_001104595.1:p.Leu972Val
|
|
NM_015075.1:c.2299C>G
|
NP_055890.1:p.Leu767Val
|
|
XM_006724579.2:c.3010C>G
|
XP_006724642.1:p.Leu1004Val
|
|
XM_006724580.2:c.2299C>G
|
XP_006724643.1:p.Leu767Val
|
|
XM_006724581.2:c.3010C>G
|
XP_006724644.1:p.Leu1004Val
|
|
XM_006724582.2:c.3010C>G
|
XP_006724645.1:p.Leu1004Val
|
|
XM_006724583.2:c.3010C>G
|
XP_006724646.1:p.Leu1004Val
|
|
XM_006724584.2:c.3010C>G
|
XP_006724647.1:p.Leu1004Val
|
|
XM_011530772.1:c.2236C>G
|
XP_011529074.1:p.Leu746Val
|
|
XM_011530773.1:c.2203C>G
|
XP_011529075.1:p.Leu735Val
|
|
XM_011530774.1:c.3010C>G
|
XP_011529076.1:p.Leu1004Val
|
|
XM_011530775.1:c.3010C>G
|
XP_011529077.1:p.Leu1004Val
|
|
XM_011530776.1:c.3010C>G
|
XP_011529078.1:p.Leu1004Val
|
|
XM_011530777.1:c.3010C>G
|
XP_011529079.1:p.Leu1004Val
|
|
XR_938365.1:n.3237C>G
|
|
|
XM_006724579.3:c.3010C>G
|
XP_006724642.1:p.Leu1004Val
|
|
XM_006724580.3:c.2299C>G
|
XP_006724643.1:p.Leu767Val
|
|
XM_006724581.4:c.3010C>G
|
XP_006724644.1:p.Leu1004Val
|
|
XM_006724582.4:c.3010C>G
|
XP_006724645.1:p.Leu1004Val
|
|
XM_006724583.4:c.3010C>G
|
XP_006724646.1:p.Leu1004Val
|
|
XM_006724584.3:c.3010C>G
|
XP_006724647.1:p.Leu1004Val
|
|
XM_011530773.2:c.2203C>G
|
XP_011529075.1:p.Leu735Val
|
|
XM_011530774.3:c.3010C>G
|
XP_011529076.1:p.Leu1004Val
|
|
XM_011530776.2:c.3010C>G
|
XP_011529078.1:p.Leu1004Val
|
|
XM_011530777.2:c.3010C>G
|
XP_011529079.1:p.Leu1004Val
|
|
XM_017029359.2:c.2884C>G
|
XP_016884848.1:p.Leu962Val
|
|
XM_017029360.1:c.2416C>G
|
XP_016884849.1:p.Leu806Val
|
|
XR_938365.2:n.3231C>G
|
|
|
NM_001111125.3:c.2914C>G
MANE Select
|
NP_001104595.1:p.Leu972Val
|
|
NM_015075.2:c.2299C>G
|
NP_055890.1:p.Leu767Val
|
|