ENST00000379644.9:c.1748A>G
MANE Select
|
ENSP00000368965.4:p.Tyr583Cys
|
|
ENST00000379644.8:c.1748A>G
|
ENSP00000368965.4:p.Tyr583Cys
|
|
ENST00000519705.1:n.1064A>G
|
|
|
ENST00000521576.1:c.899A>G
|
ENSP00000429029.1:p.Tyr300Cys
|
|
NM_152419.2:c.1748A>G
|
NP_689632.2:p.Tyr583Cys
|
|
XM_005273409.1:c.1859A>G
|
XP_005273466.1:p.Tyr620Cys
|
|
XM_005273410.1:c.1835A>G
|
XP_005273467.1:p.Tyr612Cys
|
|
XM_005273411.1:c.1667A>G
|
XP_005273468.1:p.Tyr556Cys
|
|
NM_001363227.1:c.1835A>G
|
NP_001350156.1:p.Tyr612Cys
|
|
NM_001363228.1:c.1556A>G
|
NP_001350157.1:p.Tyr519Cys
|
|
NM_001363229.1:c.884A>G
|
NP_001350158.1:p.Tyr295Cys
|
|
NM_152419.3:c.1748A>G
MANE Select
|
NP_689632.2:p.Tyr583Cys
|
|
NM_001363227.2:c.1835A>G
|
NP_001350156.1:p.Tyr612Cys
|
|
NM_001363228.2:c.1556A>G
|
NP_001350157.1:p.Tyr519Cys
|
|
NM_001363229.2:c.884A>G
|
NP_001350158.1:p.Tyr295Cys
|
|