ENST00000396623.8:c.1023G>T
MANE Select
|
ENSP00000379865.3:p.Lys341Asn
|
|
ENST00000648156.1:c.*242G>T
|
ENSP00000497007.1:n.*242G>T
|
|
ENST00000276576.11:c.*859G>T
|
ENSP00000276576.7:n.*859G>T
|
|
ENST00000396623.7:c.1023G>T
|
ENSP00000379865.3:p.Lys341Asn
|
|
ENST00000415254.5:c.879G>T
|
ENSP00000407115.1:p.Lys293Asn
|
|
ENST00000419955.5:c.*1032G>T
|
ENSP00000392040.1:n.*1032G>T
|
|
ENST00000424777.6:c.*460G>T
|
ENSP00000410883.2:n.*460G>T
|
|
ENST00000426810.5:c.*1208G>T
|
ENSP00000406905.1:n.*1208G>T
|
|
ENST00000480040.5:n.98G>T
|
|
|
ENST00000496501.5:n.897G>T
|
|
|
NM_144650.2:c.1023G>T
|
NP_653251.2:p.Lys341Asn
|
|
NM_144650.3:c.1023G>T
MANE Select
|
NP_653251.2:p.Lys341Asn
|
|