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NM_000975.5:c.121G>T
MANE Select
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NP_000966.2:p.Glu41Ter
|
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ENST00000643754.2:c.121G>T
MANE Select
|
ENSP00000496250.1:p.Glu41Ter
|
|
NM_000975.3:c.121G>T
|
NP_000966.2:p.Glu41Ter
|
|
NM_001199802.1:c.118G>T
|
NP_001186731.1:p.Glu40Ter
|
|
ENST00000374550.7:c.121G>T
|
ENSP00000363676.3:p.Glu41Ter
|
|
ENST00000374550.8:c.118G>T
|
ENSP00000363676.4:p.Glu40Ter
|
|
ENST00000443624.5:c.115G>T
|
ENSP00000390839.1:p.Glu39Ter
|
|
ENST00000443624.6:n.139G>T
|
|
|
ENST00000458455.1:c.115G>T
|
ENSP00000398888.1:p.Glu39Ter
|
|
ENST00000458455.2:c.88G>T
|
ENSP00000398888.2:p.Glu30Ter
|
|
ENST00000467075.1:n.341G>T
|
|
|
ENST00000467075.2:c.*217G>T
|
ENSP00000493634.1:n.*217G>T
|
|
ENST00000482370.1:n.418G>T
|
|
|
ENST00000482370.2:n.115G>T
|
|