ENST00000333725.10:c.1127G>A
MANE Select
|
ENSP00000331057.6:p.Trp376Ter
|
|
ENST00000267811.9:c.1127G>A
|
ENSP00000267811.5:p.Trp376Ter
|
|
ENST00000333725.9:c.1127G>A
|
ENSP00000331057.5:p.Trp376Ter
|
|
ENST00000343827.7:c.617G>A
|
ENSP00000342459.3:p.Trp206Ter
|
|
ENST00000438423.6:c.1127G>A
|
ENSP00000388940.2:p.Trp376Ter
|
|
ENST00000537840.5:c.419G>A
|
ENSP00000444696.1:p.Trp140Ter
|
|
ENST00000543579.5:c.617G>A
|
ENSP00000440017.1:p.Trp206Ter
|
|
ENST00000557843.5:c.1127G>A
|
ENSP00000453737.1:p.Trp376Ter
|
|
ENST00000558210.5:n.194G>A
|
|
|
ENST00000559609.5:c.1115G>A
|
ENSP00000453876.1:p.Trp372Ter
|
|
ENST00000559703.1:c.29G>A
|
ENSP00000454102.1:p.Trp10Ter
|
|
ENST00000559710.5:c.29G>A
|
ENSP00000453264.1:p.Trp10Ter
|
|
ENST00000560190.5:n.403-21668G>A
|
|
|
ENST00000560506.5:n.79G>A
|
|
|
ENST00000560764.5:n.962G>A
|
|
|
ENST00000561420.5:n.53G>A
|
|
|
NM_001306219.1:c.617G>A
|
NP_001293148.1:p.Trp206Ter
|
|
NM_001306220.1:c.419G>A
|
NP_001293149.1:p.Trp140Ter
|
|
NM_003205.3:c.1127G>A
|
NP_003196.1:p.Trp376Ter
|
|
NM_207036.1:c.1127G>A
|
NP_996919.1:p.Trp376Ter
|
|
NM_207037.1:c.1127G>A
|
NP_996920.1:p.Trp376Ter
|
|
NM_207038.1:c.1127G>A
|
NP_996921.1:p.Trp376Ter
|
|
NM_207040.1:c.617G>A
|
NP_996923.1:p.Trp206Ter
|
|
XM_005254613.3:c.953G>A
|
XP_005254670.1:p.Trp318Ter
|
|
XM_011521959.1:c.1163G>A
|
XP_011520261.1:p.Trp388Ter
|
|
XM_011521960.1:c.1163G>A
|
XP_011520262.1:p.Trp388Ter
|
|
XM_011521961.1:c.1163G>A
|
XP_011520263.1:p.Trp388Ter
|
|
XM_011521962.1:c.1163G>A
|
XP_011520264.1:p.Trp388Ter
|
|
XM_011521963.1:c.1163G>A
|
XP_011520265.1:p.Trp388Ter
|
|
XM_011521965.1:c.479G>A
|
XP_011520267.1:p.Trp160Ter
|
|
XM_011521966.1:c.419G>A
|
XP_011520268.1:p.Trp140Ter
|
|
XM_011521967.1:c.479G>A
|
XP_011520269.1:p.Trp160Ter
|
|
XM_011521969.1:c.617G>A
|
XP_011520271.1:p.Trp206Ter
|
|
NM_001306219.2:c.617G>A
|
NP_001293148.1:p.Trp206Ter
|
|
NM_001306220.2:c.419G>A
|
NP_001293149.1:p.Trp140Ter
|
|
NM_001322151.1:c.1127G>A
|
NP_001309080.1:p.Trp376Ter
|
|
NM_001322152.1:c.1127G>A
|
NP_001309081.1:p.Trp376Ter
|
|
NM_001322154.1:c.470G>A
|
NP_001309083.1:p.Trp157Ter
|
|
NM_001322156.1:c.953G>A
|
NP_001309085.1:p.Trp318Ter
|
|
NM_001322157.1:c.1127G>A
|
NP_001309086.1:p.Trp376Ter
|
|
NM_001322158.1:c.953G>A
|
NP_001309087.1:p.Trp318Ter
|
|
NM_001322159.1:c.1127G>A
|
NP_001309088.1:p.Trp376Ter
|
|
NM_001322161.1:c.1127G>A
|
NP_001309090.1:p.Trp376Ter
|
|
NM_001322162.1:c.1127G>A
|
NP_001309091.1:p.Trp376Ter
|
|
NM_001322164.1:c.1163G>A
|
NP_001309093.1:p.Trp388Ter
|
|
NM_001322165.1:c.1127G>A
|
NP_001309094.1:p.Trp376Ter
|
|
XM_011521959.3:c.1163G>A
|
XP_011520261.1:p.Trp388Ter
|
|
XM_011521960.3:c.1163G>A
|
XP_011520262.1:p.Trp388Ter
|
|
XM_011521961.3:c.1163G>A
|
XP_011520263.1:p.Trp388Ter
|
|
XM_011521962.3:c.1163G>A
|
XP_011520264.1:p.Trp388Ter
|
|
XM_011521963.3:c.1163G>A
|
XP_011520265.1:p.Trp388Ter
|
|
XM_011521965.2:c.479G>A
|
XP_011520267.1:p.Trp160Ter
|
|
XM_011521966.2:c.419G>A
|
XP_011520268.1:p.Trp140Ter
|
|
XM_011521967.2:c.479G>A
|
XP_011520269.1:p.Trp160Ter
|
|
XM_017022520.2:c.1127G>A
|
XP_016878009.1:p.Trp376Ter
|
|
NM_001306219.3:c.617G>A
|
NP_001293148.1:p.Trp206Ter
|
|
NM_001306220.3:c.419G>A
|
NP_001293149.1:p.Trp140Ter
|
|
NM_001322152.2:c.1127G>A
|
NP_001309081.1:p.Trp376Ter
|
|
NM_001322154.2:c.470G>A
|
NP_001309083.1:p.Trp157Ter
|
|
NM_001322156.2:c.953G>A
|
NP_001309085.1:p.Trp318Ter
|
|
NM_001322157.2:c.1127G>A
|
NP_001309086.1:p.Trp376Ter
|
|
NM_001322158.2:c.953G>A
|
NP_001309087.1:p.Trp318Ter
|
|
NM_001322159.2:c.1127G>A
|
NP_001309088.1:p.Trp376Ter
|
|
NM_001322161.2:c.1127G>A
|
NP_001309090.1:p.Trp376Ter
|
|
NM_001322162.2:c.1127G>A
|
NP_001309091.1:p.Trp376Ter
|
|
NM_001322164.2:c.1163G>A
|
NP_001309093.1:p.Trp388Ter
|
|
NM_001322165.2:c.1127G>A
|
NP_001309094.1:p.Trp376Ter
|
|
NM_003205.4:c.1127G>A
|
NP_003196.1:p.Trp376Ter
|
|
NM_207036.2:c.1127G>A
|
NP_996919.1:p.Trp376Ter
|
|
NM_207037.2:c.1127G>A
MANE Select
|
NP_996920.1:p.Trp376Ter
|
|
NM_207038.2:c.1127G>A
|
NP_996921.1:p.Trp376Ter
|
|
NM_207040.2:c.617G>A
|
NP_996923.1:p.Trp206Ter
|
|
NM_001322151.2:c.1127G>A
|
NP_001309080.1:p.Trp376Ter
|
|
NM_001322157.3:c.1127G>A
|
NP_001309086.1:p.Trp376Ter
|
|
NM_001322159.3:c.1127G>A
|
NP_001309088.1:p.Trp376Ter
|
|