ENST00000218099.7:c.1053C>T
MANE Select
|
ENSP00000218099.2:p.Gly351=
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ENST00000643157.1:n.1720C>T
|
|
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ENST00000218099.6:c.1053C>T
|
ENSP00000218099.2:p.Gly351=
|
|
ENST00000394090.2:c.939C>T
|
ENSP00000377650.2:p.Gly313=
|
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NM_000133.3:c.1053C>T , LRG_556t1:c.1053C>T
|
NP_000124.1:p.Gly351=
|
|
NM_001313913.1:c.939C>T
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NP_001300842.1:p.Gly313=
|
|
XM_005262397.3:c.924C>T
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XP_005262454.1:p.Gly308=
|
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XM_005262397.4:c.924C>T
|
XP_005262454.1:p.Gly308=
|
|
NM_000133.4:c.1053C>T
MANE Select
|
NP_000124.1:p.Gly351=
|
|
NM_001313913.2:c.939C>T
|
NP_001300842.1:p.Gly313=
|
|