|
NM_003322.6:c.139G>T
MANE Select
|
NP_003313.3:p.Glu47Ter
|
|
ENST00000229771.11:c.139G>T
MANE Select
|
ENSP00000229771.6:p.Glu47Ter
|
|
NM_001289395.1:c.139G>T
|
NP_001276324.1:p.Glu47Ter
|
|
NM_001289395.2:c.139G>T
|
NP_001276324.1:p.Glu47Ter
|
|
NM_003322.4:c.139G>T
|
NP_003313.3:p.Glu47Ter
|
|
NM_003322.5:c.139G>T
|
NP_003313.3:p.Glu47Ter
|
|
ENST00000229771.10:c.139G>T
|
ENSP00000229771.6:p.Glu47Ter
|
|
ENST00000322263.8:c.139G>T
|
ENSP00000319414.4:p.Glu47Ter
|
|
ENST00000428978.1:c.139G>T
|
ENSP00000406765.1:p.Glu47Ter
|
|
ENST00000448446.2:n.44G>T
|
|
|
ENST00000614066.4:c.139G>T
|
ENSP00000477534.1:p.Glu47Ter
|