ENST00000471889.7:c.662T>G
MANE Select
|
ENSP00000418096.3:p.Val221Gly
|
|
ENST00000289877.8:c.662T>G
|
ENSP00000289877.8:p.Val221Gly
|
|
ENST00000471889.5:c.764T>G
|
ENSP00000418096.2:p.Val255Gly
|
|
NM_001080397.2:c.764T>G
|
NP_001073866.2:p.Val255Gly
|
|
XM_011541530.1:c.764T>G
|
XP_011539832.1:p.Val255Gly
|
|
XM_011541531.1:c.671T>G
|
XP_011539833.1:p.Val224Gly
|
|
XM_011541530.2:c.764T>G
|
XP_011539832.1:p.Val255Gly
|
|
XM_011541531.2:c.671T>G
|
XP_011539833.1:p.Val224Gly
|
|
XM_024447371.1:c.671T>G
|
XP_024303139.1:p.Val224Gly
|
|
XM_024447372.1:c.56T>G
|
XP_024303140.1:p.Val19Gly
|
|
NM_001080397.3:c.662T>G
MANE Select
|
NP_001073866.3:p.Val221Gly
|
|
NM_001379614.1:c.662T>G
|
NP_001366543.1:p.Val221Gly
|
|
NM_001379615.1:c.569T>G
|
NP_001366544.1:p.Val190Gly
|
|
NM_001379616.1:c.569T>G
|
NP_001366545.1:p.Val190Gly
|
|
NM_001379617.1:c.56T>G
|
NP_001366546.1:p.Val19Gly
|
|
NM_001379618.1:c.56T>G
|
NP_001366547.1:p.Val19Gly
|
|