ENST00000218099.7:c.677G=
MANE Select
|
ENSP00000218099.2:p.Arg226=
|
|
ENST00000643157.1:n.1344G=
|
|
|
ENST00000218099.6:c.677G=
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ENSP00000218099.2:p.Arg226=
|
|
ENST00000394090.2:c.563G=
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ENSP00000377650.2:p.Arg188=
|
|
NM_000133.3:c.677G= , LRG_556t1:c.677G=
|
NP_000124.1:p.Arg226=
|
|
NM_001313913.1:c.563G=
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NP_001300842.1:p.Arg188=
|
|
XM_005262397.3:c.548G=
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XP_005262454.1:p.Arg183=
|
|
XM_005262397.4:c.548G=
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XP_005262454.1:p.Arg183=
|
|
NM_000133.4:c.677G=
MANE Select
|
NP_000124.1:p.Arg226=
|
|
NM_001313913.2:c.563G=
|
NP_001300842.1:p.Arg188=
|
|