ENST00000682114.1:c.124G>T
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ENSP00000507245.1:p.Glu42Ter
|
|
ENST00000682478.1:n.100G>T
|
|
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ENST00000683576.1:n.100G>T
|
|
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ENST00000683627.1:c.124G>T
|
ENSP00000507533.1:p.Glu42Ter
|
|
ENST00000684082.1:c.124G>T
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ENSP00000508266.1:p.Glu42Ter
|
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ENST00000684633.1:n.96G>T
|
|
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ENST00000684678.1:c.120G>T
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ENSP00000507059.1:p.Thr40=
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ENST00000369842.9:c.124G>T
MANE Select
|
ENSP00000358857.4:p.Glu42Ter
|
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ENST00000369835.3:c.82+165G>T
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ENSP00000358850.3:n.82+165G>T
|
|
ENST00000369842.8:c.124G>T
|
ENSP00000358857.4:p.Glu42Ter
|
|
ENST00000428228.5:c.*29G>T
|
ENSP00000401081.1:n.*29G>T
|
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ENST00000468294.5:n.84G>T
|
|
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ENST00000485261.1:n.163+165G>T
|
|
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ENST00000486738.5:n.268G>T
|
|
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ENST00000492448.1:n.107G>T
|
|
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ENST00000494443.5:n.181G>T
|
|
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NM_000117.2:c.124G>T , LRG_745t1:c.124G>T
|
NP_000108.1:p.Glu42Ter
|
|
XM_024452349.1:c.-85G>T
|
XP_024308117.1:n.-85G>T
|
|
NM_000117.3:c.124G>T
MANE Select
|
NP_000108.1:p.Glu42Ter
|
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