ENST00000643051.1:c.2269G>T
|
ENSP00000495513.1:p.Glu757Ter
|
|
ENST00000643556.1:c.2410G>T
|
ENSP00000494938.1:n.2410G>T
|
|
ENST00000643816.1:n.2552G>T
|
|
|
ENST00000643842.1:c.*2315G>T
|
ENSP00000493861.1:n.*2315G>T
|
|
ENST00000645237.2:c.2269G>T
MANE Select
|
ENSP00000494609.1:p.Glu757Ter
|
|
ENST00000646439.1:c.2128G>T
|
ENSP00000494751.1:p.Glu710Ter
|
|
ENST00000376887.8:c.2269G>T
|
ENSP00000366084.4:p.Glu757Ter
|
|
ENST00000536256.3:c.2044G>T
|
ENSP00000442024.1:p.Glu682Ter
|
|
ENST00000629385.1:c.2269G>T
|
ENSP00000487081.1:p.Glu757Ter
|
|
NM_001105515.2:c.2269G>T
|
NP_001098985.1:p.Glu757Ter
|
|
NM_001301829.1:c.2128G>T
|
NP_001288758.1:p.Glu710Ter
|
|
NM_001301830.1:c.2044G>T
|
NP_001288759.1:p.Glu682Ter
|
|
NM_005845.4:c.2269G>T
|
NP_005836.2:p.Glu757Ter
|
|
XM_005254025.2:c.2140G>T
|
XP_005254082.1:p.Glu714Ter
|
|
XM_006719914.1:c.2179G>T
|
XP_006719977.1:p.Glu727Ter
|
|
XM_011521047.1:c.1720G>T
|
XP_011519349.1:p.Glu574Ter
|
|
XM_017020319.1:c.2140G>T
|
XP_016875808.1:p.Glu714Ter
|
|
XM_017020320.2:c.2269G>T
|
XP_016875809.1:p.Glu757Ter
|
|
XM_017020321.1:c.754G>T
|
XP_016875810.1:p.Glu252Ter
|
|
XM_017020322.1:c.2140G>T
|
XP_016875811.1:p.Glu714Ter
|
|
NM_001105515.3:c.2269G>T
|
NP_001098985.1:p.Glu757Ter
|
|
NM_001301829.2:c.2128G>T
|
NP_001288758.1:p.Glu710Ter
|
|
NM_001301830.2:c.2044G>T
|
NP_001288759.1:p.Glu682Ter
|
|
NM_005845.5:c.2269G>T
MANE Select
|
NP_005836.2:p.Glu757Ter
|
|