ENST00000395796.8:c.*987T=
|
ENSP00000379142.4:n.*987T=
|
|
ENST00000616242.5:c.*109T=
|
ENSP00000482149.2:n.*109T=
|
|
ENST00000683378.1:n.215T=
|
|
|
ENST00000345378.7:c.992T=
|
ENSP00000223366.2:p.Phe331=
|
|
ENST00000403799.8:c.989T=
MANE Select
|
ENSP00000384247.3:p.Phe330=
|
|
ENST00000671824.1:c.1052T=
|
ENSP00000500264.1:p.Phe351=
|
|
ENST00000673284.1:c.989T=
|
ENSP00000499852.1:p.Phe330=
|
|
ENST00000345378.6:c.992T=
|
ENSP00000223366.2:p.Phe331=
|
|
ENST00000395796.7:c.986T=
|
ENSP00000379142.3:p.Phe329=
|
|
ENST00000403799.7:c.989T=
|
ENSP00000384247.3:p.Phe330=
|
|
ENST00000437084.1:c.938T=
|
ENSP00000402840.1:p.Phe313=
|
|
ENST00000473353.1:n.287T=
|
|
|
ENST00000616242.4:c.986T=
|
ENSP00000482149.1:p.Phe329=
|
|
NM_000162.3:c.989T=
|
NP_000153.1:p.Phe330=
|
|
NM_033507.1:c.992T=
|
NP_277042.1:p.Phe331=
|
|
NM_033508.1:c.986T=
|
NP_277043.1:p.Phe329=
|
|
NM_000162.4:c.989T=
|
NP_000153.1:p.Phe330=
|
|
NM_001354800.1:c.989T=
|
NP_001341729.1:p.Phe330=
|
|
NM_001354801.1:c.8+126T=
|
NP_001341730.1:n.8+126T=
|
|
NM_033507.2:c.992T=
|
NP_277042.1:p.Phe331=
|
|
NM_033508.2:c.986T=
|
NP_277043.1:p.Phe329=
|
|
NM_000162.5:c.989T=
MANE Select
|
NP_000153.1:p.Phe330=
|
|
NM_033507.3:c.992T=
|
NP_277042.1:p.Phe331=
|
|
NM_033508.3:c.986T=
|
NP_277043.1:p.Phe329=
|
|