ENST00000368985.8:c.919G>T
MANE Select
|
ENSP00000357981.3:p.Glu307Ter
|
|
ENST00000448301.7:c.691G>T
|
ENSP00000408414.2:p.Glu231Ter
|
|
ENST00000472977.7:c.919G>T
|
ENSP00000475176.2:p.Glu307Ter
|
|
ENST00000483930.2:c.*113G>T
|
ENSP00000475812.2:n.*113G>T
|
|
ENST00000607427.2:c.919G>T
|
ENSP00000475557.2:p.Glu307Ter
|
|
ENST00000679512.1:c.816G>T
|
ENSP00000505113.1:p.Lys272Asn
|
|
ENST00000679898.1:c.646G>T
|
ENSP00000505326.1:p.Glu216Ter
|
|
ENST00000680288.1:c.769G>T
|
ENSP00000506001.1:p.Glu257Ter
|
|
ENST00000680311.1:c.*2G>T
|
ENSP00000505020.1:n.*2G>T
|
|
ENST00000680471.1:c.*90G>T
|
ENSP00000506603.1:n.*90G>T
|
|
ENST00000680664.1:c.742G>T
|
ENSP00000506248.1:p.Glu248Ter
|
|
ENST00000680931.1:c.*269G>T
|
ENSP00000504934.1:n.*269G>T
|
|
ENST00000681357.1:n.309G>T
|
|
|
ENST00000681444.1:c.919G>T
|
ENSP00000505359.1:p.Glu307Ter
|
|
ENST00000368985.7:c.919G>T
|
ENSP00000357981.3:p.Glu307Ter
|
|
ENST00000448301.6:c.769G>T
|
ENSP00000408414.1:p.Glu257Ter
|
|
ENST00000472977.6:c.212G>T
|
|
|
ENST00000483930.1:c.467G>T
|
ENSP00000475812.1:n.467G>T
|
|
NM_001199739.1:c.769G>T
|
NP_001186668.1:p.Glu257Ter
|
|
NM_004079.4:c.919G>T
|
NP_004070.3:p.Glu307Ter
|
|
NM_004079.5:c.919G>T
MANE Select
|
NP_004070.3:p.Glu307Ter
|
|
NM_001199739.2:c.769G>T
|
NP_001186668.1:p.Glu257Ter
|
|