ENST00000230771.9:c.615G>T
MANE Select
|
ENSP00000230771.3:p.Leu205Phe
|
|
ENST00000503873.6:c.393G>T
|
ENSP00000424516.2:p.Leu131Phe
|
|
ENST00000509299.6:c.405G>T
|
ENSP00000425695.2:p.Leu135Phe
|
|
ENST00000520095.6:c.*193G>T
|
ENSP00000429220.1:n.*193G>T
|
|
ENST00000642452.1:c.581G>T
|
|
|
ENST00000642752.1:c.615G>T
|
ENSP00000493630.1:p.Leu205Phe
|
|
ENST00000642970.1:c.405G>T
|
ENSP00000496011.1:p.Leu135Phe
|
|
ENST00000643996.1:c.405G>T
|
ENSP00000495350.1:p.Leu135Phe
|
|
ENST00000645065.1:c.633G>T
|
ENSP00000493571.1:p.Leu211Phe
|
|
ENST00000645749.1:c.615G>T
|
ENSP00000494296.1:p.Leu205Phe
|
|
ENST00000646468.1:c.633G>T
|
ENSP00000494965.1:p.Leu211Phe
|
|
ENST00000647484.1:c.405G>T
|
ENSP00000494140.1:p.Leu135Phe
|
|
ENST00000230771.7:c.615G>T
|
ENSP00000230771.3:p.Leu205Phe
|
|
ENST00000448069.2:c.198G>T
|
ENSP00000407105.2:p.Leu66Phe
|
|
ENST00000508522.5:c.540G>T
|
ENSP00000423616.1:p.Leu180Phe
|
|
ENST00000510104.5:c.*415G>T
|
ENSP00000423530.1:n.*415G>T
|
|
ENST00000513688.1:n.622G>T
|
|
|
NM_001278731.1:c.540G>T
|
NP_001265660.1:p.Leu180Phe
|
|
NM_001278732.1:c.183G>T
|
NP_001265661.1:p.Leu61Phe
|
|
NM_012208.3:c.615G>T
|
NP_036340.1:p.Leu205Phe
|
|
XM_011537619.1:c.633G>T
|
XP_011535921.1:p.Leu211Phe
|
|
XM_011537620.1:c.633G>T
|
XP_011535922.1:p.Leu211Phe
|
|
NM_001363535.1:c.633G>T
|
NP_001350464.1:p.Leu211Phe
|
|
NM_001363536.1:c.405G>T
|
NP_001350465.1:p.Leu135Phe
|
|
XM_017009288.1:c.405G>T
|
XP_016864777.1:p.Leu135Phe
|
|
XM_017009289.1:c.405G>T
|
XP_016864778.1:p.Leu135Phe
|
|
XM_017009290.2:c.-120G>T
|
XP_016864779.1:n.-120G>T
|
|
XM_017009291.1:c.-120G>T
|
XP_016864780.1:n.-120G>T
|
|
XM_017009292.1:c.-120G>T
|
XP_016864781.1:n.-120G>T
|
|
NM_012208.4:c.615G>T
MANE Select
|
NP_036340.1:p.Leu205Phe
|
|
NM_001278731.2:c.540G>T
|
NP_001265660.1:p.Leu180Phe
|
|
NM_001278732.2:c.183G>T
|
NP_001265661.1:p.Leu61Phe
|
|
NM_001363535.2:c.633G>T
|
NP_001350464.1:p.Leu211Phe
|
|
NM_001363536.2:c.405G>T
|
NP_001350465.1:p.Leu135Phe
|
|