ENST00000393609.8:c.808G>T
MANE Select
|
ENSP00000377233.3:p.Gly270Ter
|
|
ENST00000334211.12:c.73G>T
|
ENSP00000335506.8:p.Gly25Ter
|
|
ENST00000359373.9:c.808G>T
|
ENSP00000352332.5:p.Gly270Ter
|
|
ENST00000393605.7:c.88G>T
|
ENSP00000377230.3:p.Gly30Ter
|
|
ENST00000393609.7:c.808G>T
|
ENSP00000377233.3:p.Gly270Ter
|
|
ENST00000426523.5:c.73G>T
|
ENSP00000392264.1:p.Gly25Ter
|
|
ENST00000429686.5:c.73G>T
|
ENSP00000403127.1:p.Gly25Ter
|
|
ENST00000465814.5:n.1145G>T
|
|
|
NM_001040118.2:c.808G>T
|
NP_001035207.1:p.Gly270Ter
|
|
NM_001135190.1:c.73G>T
|
NP_001128662.1:p.Gly25Ter
|
|
NM_015242.4:c.73G>T
|
NP_056057.2:p.Gly25Ter
|
|
NM_001369489.1:c.73G>T
|
NP_001356418.1:p.Gly25Ter
|
|
NR_161388.1:n.790G>T
|
|
|
NM_001040118.3:c.808G>T
MANE Select
|
NP_001035207.1:p.Gly270Ter
|
|
NM_001135190.2:c.73G>T
|
NP_001128662.1:p.Gly25Ter
|
|
NM_015242.5:c.73G>T
|
NP_056057.2:p.Gly25Ter
|
|