|
NM_015375.3:c.1477G>T
MANE Select
|
NP_056190.1:p.Gly493Ter
|
|
ENST00000367162.8:c.1477G>T
MANE Select
|
ENSP00000356130.3:p.Gly493Ter
|
|
NM_015375.2:c.1477G>T
|
NP_056190.1:p.Gly493Ter
|
|
NM_199462.2:c.1477G>T
|
NP_955749.1:p.Gly493Ter
|
|
NM_199462.3:c.1477G>T
|
NP_955749.1:p.Gly493Ter
|
|
ENST00000367161.7:c.1477G>T
|
ENSP00000356129.3:p.Gly493Ter
|
|
ENST00000367162.7:c.1477G>T
|
ENSP00000356130.3:p.Gly493Ter
|
|
ENST00000615388.1:c.-89-52G>T
|
ENSP00000478016.1:n.-89-52G>T
|
|
XM_011509392.1:c.1450G>T
|
XP_011507694.1:p.Gly484Ter
|
|
XM_011509392.2:c.1450G>T
|
XP_011507694.1:p.Gly484Ter
|
|
XM_011509393.1:c.892G>T
|
XP_011507695.1:p.Gly298Ter
|
|
XM_011509393.2:c.892G>T
|
XP_011507695.1:p.Gly298Ter
|
|
XM_011509394.1:c.850G>T
|
XP_011507696.1:p.Gly284Ter
|
|
XM_011509394.2:c.850G>T
|
XP_011507696.1:p.Gly284Ter
|