ENST00000302804.12:c.618G>T
MANE Select
|
ENSP00000302898.6:p.Leu206Phe
|
|
ENST00000302804.11:c.618G>T
|
ENSP00000302898.6:p.Leu206Phe
|
|
ENST00000415300.6:c.561G>T
|
ENSP00000407162.1:p.Leu187Phe
|
|
ENST00000448930.5:c.513G>T
|
ENSP00000406798.2:p.Leu171Phe
|
|
ENST00000594599.1:c.102G>T
|
ENSP00000469894.1:p.Leu34Phe
|
|
ENST00000596375.1:c.*179G>T
|
ENSP00000470465.1:n.*179G>T
|
|
ENST00000598785.5:c.516G>T
|
ENSP00000471830.1:p.Leu172Phe
|
|
ENST00000599062.5:c.609G>T
|
ENSP00000469983.1:p.Leu203Phe
|
|
ENST00000601799.5:c.*917G>T
|
ENSP00000468918.1:n.*917G>T
|
|
NM_001015878.1:c.618G>T
|
NP_001015878.1:p.Leu206Phe
|
|
NM_001015879.1:c.561G>T
|
NP_001015879.1:p.Leu187Phe
|
|
NM_003160.2:c.516G>T
|
NP_003151.2:p.Leu172Phe
|
|
XR_430209.2:n.1512G>T
|
|
|
XR_430209.3:n.1555G>T
|
|
|
NM_001015878.2:c.618G>T
MANE Select
|
NP_001015878.1:p.Leu206Phe
|
|
NM_001015879.2:c.561G>T
|
NP_001015879.1:p.Leu187Phe
|
|
NM_003160.3:c.516G>T
|
NP_003151.2:p.Leu172Phe
|
|