ENST00000395796.8:c.*563A>G
|
ENSP00000379142.4:n.*563A>G
|
|
ENST00000616242.5:c.565A>G
|
ENSP00000482149.2:p.Ile189Val
|
|
ENST00000682635.1:n.1051A>G
|
|
|
ENST00000345378.7:c.568A>G
|
ENSP00000223366.2:p.Ile190Val
|
|
ENST00000403799.8:c.565A>G
MANE Select
|
ENSP00000384247.3:p.Ile189Val
|
|
ENST00000671824.1:c.565A>G
|
ENSP00000500264.1:p.Ile189Val
|
|
ENST00000673284.1:c.565A>G
|
ENSP00000499852.1:p.Ile189Val
|
|
ENST00000345378.6:c.568A>G
|
ENSP00000223366.2:p.Ile190Val
|
|
ENST00000395796.7:c.562A>G
|
ENSP00000379142.3:p.Ile188Val
|
|
ENST00000403799.7:c.565A>G
|
ENSP00000384247.3:p.Ile189Val
|
|
ENST00000437084.1:c.514A>G
|
ENSP00000402840.1:p.Ile172Val
|
|
ENST00000616242.4:c.562A>G
|
ENSP00000482149.1:p.Ile188Val
|
|
NM_000162.3:c.565A>G
|
NP_000153.1:p.Ile189Val
|
|
NM_033507.1:c.568A>G
|
NP_277042.1:p.Ile190Val
|
|
NM_033508.1:c.562A>G
|
NP_277043.1:p.Ile188Val
|
|
NM_000162.4:c.565A>G
|
NP_000153.1:p.Ile189Val
|
|
NM_001354800.1:c.565A>G
|
NP_001341729.1:p.Ile189Val
|
|
NM_033507.2:c.568A>G
|
NP_277042.1:p.Ile190Val
|
|
NM_033508.2:c.562A>G
|
NP_277043.1:p.Ile188Val
|
|
NM_000162.5:c.565A>G
MANE Select
|
NP_000153.1:p.Ile189Val
|
|
NM_033507.3:c.568A>G
|
NP_277042.1:p.Ile190Val
|
|
NM_033508.3:c.562A>G
|
NP_277043.1:p.Ile188Val
|
|