ENST00000422737.7:c.1445G>A
|
ENSP00000415650.3:p.Arg482Lys
|
|
ENST00000334344.11:c.1445G>A
MANE Select
|
ENSP00000335044.6:p.Arg482Lys
|
|
ENST00000422737.6:c.1366G>A
|
|
|
ENST00000334344.10:c.1445G>A
|
ENSP00000335044.6:p.Arg482Lys
|
|
ENST00000422737.5:c.998G>A
|
ENSP00000415650.1:p.Arg333Lys
|
|
ENST00000444670.5:c.275G>A
|
ENSP00000397307.1:p.Arg92Lys
|
|
ENST00000479608.5:n.653G>A
|
|
|
ENST00000480128.1:n.469G>A
|
|
|
NM_152641.2:c.1445G>A
|
NP_689854.2:p.Arg482Lys
|
|
XM_006719272.2:c.1445G>A
|
XP_006719335.1:p.Arg482Lys
|
|
XM_011538025.1:c.-271G>A
|
XP_011536327.1:n.-271G>A
|
|
XR_944505.1:n.1593G>A
|
|
|
XR_944892.1:n.289+409C>T
|
|
|
XR_944893.1:n.289+409C>T
|
|
|
NM_001347839.1:c.1445G>A
|
NP_001334768.1:p.Arg482Lys
|
|
NM_152641.3:c.1445G>A
|
NP_689854.2:p.Arg482Lys
|
|
XM_006719272.4:c.1445G>A
|
XP_006719335.1:p.Arg482Lys
|
|
XR_001749098.1:n.476+409C>T
|
|
|
XR_944505.3:n.1576G>A
|
|
|
XR_944892.2:n.289+409C>T
|
|
|
NM_152641.4:c.1445G>A
MANE Select
|
NP_689854.2:p.Arg482Lys
|
|
NM_001347839.2:c.1445G>A
|
NP_001334768.1:p.Arg482Lys
|
|