ENST00000697641.1:n.2448G>T
|
|
|
ENST00000697642.1:c.412G>T
|
ENSP00000513368.1:p.Glu138Ter
|
|
ENST00000697643.1:c.412G>T
|
ENSP00000513369.1:p.Glu138Ter
|
|
ENST00000697644.1:n.2580G>T
|
|
|
ENST00000336787.6:c.412G>T
MANE Select
|
ENSP00000337761.1:p.Glu138Ter
|
|
ENST00000336787.5:c.412G>T
|
ENSP00000337761.1:p.Glu138Ter
|
|
ENST00000396307.6:c.412G>T
|
ENSP00000379601.2:p.Glu138Ter
|
|
ENST00000564609.5:c.412G>T
|
ENSP00000455012.1:p.Glu138Ter
|
|
ENST00000566877.5:c.412G>T
|
ENSP00000454695.1:p.Glu138Ter
|
|
ENST00000567380.5:c.412G>T
|
ENSP00000458127.1:p.Glu138Ter
|
|
ENST00000569493.5:c.412G>T
|
ENSP00000456059.1:p.Glu138Ter
|
|
NM_004580.4:c.412G>T
|
NP_004571.2:p.Glu138Ter
|
|
NM_183234.2:c.412G>T
|
NP_899057.1:p.Glu138Ter
|
|
NM_183235.2:c.412G>T
|
NP_899058.1:p.Glu138Ter
|
|
NM_183236.2:c.412G>T
|
NP_899059.1:p.Glu138Ter
|
|
XM_005254576.3:c.412G>T
|
XP_005254633.1:p.Glu138Ter
|
|
XM_011521852.1:c.412G>T
|
XP_011520154.1:p.Glu138Ter
|
|
XM_011521853.1:c.412G>T
|
XP_011520155.1:p.Glu138Ter
|
|
XM_011521854.1:c.412G>T
|
XP_011520156.1:p.Glu138Ter
|
|
XM_011521855.1:c.412G>T
|
XP_011520157.1:p.Glu138Ter
|
|
XM_011521856.1:c.412G>T
|
XP_011520158.1:p.Glu138Ter
|
|
XM_005254576.5:c.412G>T
|
XP_005254633.1:p.Glu138Ter
|
|
XM_011521855.3:c.412G>T
|
XP_011520157.1:p.Glu138Ter
|
|
XM_011521856.2:c.412G>T
|
XP_011520158.1:p.Glu138Ter
|
|
XM_024450009.1:c.412G>T
|
XP_024305777.1:p.Glu138Ter
|
|
NM_183235.3:c.412G>T
MANE Select
|
NP_899058.1:p.Glu138Ter
|
|
NM_004580.5:c.412G>T
|
NP_004571.2:p.Glu138Ter
|
|
NM_183236.3:c.412G>T
|
NP_899059.1:p.Glu138Ter
|
|