ENST00000333590.6:c.276G>T
MANE Select
|
ENSP00000369820.3:p.Leu92Phe
|
|
ENST00000637296.1:c.-315+219G>T
|
ENSP00000490545.1:n.-315+219G>T
|
|
ENST00000637626.1:c.276G>T
|
ENSP00000489928.1:p.Leu92Phe
|
|
ENST00000638131.1:c.111+165G>T
|
ENSP00000490483.1:n.111+165G>T
|
|
ENST00000333590.5:c.276G>T
|
ENSP00000369820.3:p.Leu92Phe
|
|
ENST00000474662.2:n.142+219G>T
|
|
|
ENST00000482148.6:c.276G>T
|
ENSP00000489528.1:p.Leu92Phe
|
|
ENST00000542278.6:c.276G>T
|
ENSP00000442653.2:p.Leu92Phe
|
|
ENST00000634286.1:c.69G>T
|
ENSP00000489491.1:p.Leu23Phe
|
|
ENST00000634582.1:c.13+3846G>T
|
ENSP00000489540.1:n.13+3846G>T
|
|
ENST00000634640.1:c.-231+219G>T
|
ENSP00000489083.1:n.-231+219G>T
|
|
ENST00000635045.1:n.361G>T
|
|
|
ENST00000635543.1:c.276G>T
|
ENSP00000489205.1:p.Leu92Phe
|
|
ENST00000635598.1:c.276G>T
|
ENSP00000489207.1:p.Leu92Phe
|
|
NM_002641.3:c.276G>T , LRG_160t1:c.276G>T
|
NP_002632.1:p.Leu92Phe
|
|
NM_020473.3:c.13+3846G>T
|
NP_065206.3:n.13+3846G>T
|
|
NR_033835.1:n.392G>T
|
|
|
NR_033836.1:n.173+219G>T
|
|
|
NM_002641.4:c.276G>T
MANE Select
|
NP_002632.1:p.Leu92Phe
|
|